| 编号 | 中文名称 | 英文名称 |
|---|---|---|
| DIN 13090-4-1986 | 医疗器械用锥形接头.（经尿道前列腺）切除器用锁紧接头 | Conical fittings for medical equipment; lock fittings for resectoscopes |
| DIN 13103-2010 | 医疗器械.解剖割刀 | Medical instruments - Dissecting scalpels |
| DIN 13104-2010 | 医疗器械.软骨刀 | Medical instruments - Cartilage knife |
| DIN 13105-2010 | 医疗器械.尸体解剖刀 | Medical instruments - Autopsy knife |
| DIN 13109-2010 | 医疗器械.无合金刀片的结扎线剪 | Medical instruments - Wire cutting scissors without carbide inserts |
| DIN 13111-2006 | 医疗器械.绷带剪 | Medical instruments - Bandage scissors |
| DIN 13112-1-2006 | 医疗器械.第1部分:不镶硬质合金的解剖剪 | Medical instruments - Part 1: Scissors for preparations without carbide inserts |
| DIN 13114-1-1980 | 医疗仪器.第1部分:无镶嵌硬质合金的梅奥氏剪子 | Medical instruments; scissors type Mayo without carbide inserts |
| DIN 13115-2006 | 医疗器械.平面弯曲指甲剪 | Medical instruments - Nail scissors, curved on flat |
| DIN 13116-1980 | 医疗器械；西姆茨氏直形绷带剪 | Medical instruments; bandage scissors, Smith's, straight |
| DIN 13117-1980 | 医疗器械；骨剪 | Medical instruments; bone shears |
| DIN 13119-2010 | 医疗器械.肠剪 | Medical instruments - Bowel scissors |
| DIN 13120-2006 | 医疗器械.绷带和布用内弯曲剪刀 | Medical instruments - Bandage and clothing scissors, angled to side |
| DIN 13122-2005 | 医疗器械.1 1带齿直式钩钳 | Medical instruments - Tenaculum forceps 1 × 1 teeth, straight |
| DIN 13123-2005 | 医疗器械.2 2带齿直式双爪钳 | Medical instruments - Vulsellum forceps 2 × 2 teeth, straight |
| DIN 13128-2005 | 医疗器械.Allis型夹肠钳 | Medical instruments - Intestinal forceps type Allis |
| DIN 13129-2005 | 医疗器械.Maier型直式敷料钳 | Medical instruments - Dressing forceps type Maier, straight |
| DIN 13130-2005 | 医疗器械.Maier型弯形敷料钳 | Medical instruments - Dressing forceps type Maier, curved |
| DIN 13133-1-2005 | 医疗仪器.Sims型弯形子宫剪.第1部分:不含硬质合金镶片 | Medical instruments - Uterine scissors, curved on flat, type Sims - Part 1: Without carbide inserts |
| DIN 13134-2010 | 医疗器械.西姆斯直行子宫剪.无合金刀片 | Medical instruments - Uterine scissors, straight, type Sims - Without carbide inserts |
| DIN 13135-2010 | 医疗器械.基尔希纳式腹壁牵开器 | Medical instruments - Abdominal retractors type Kirschner |
| DIN 13137-2010 | 医疗器械.弗里契式腹壁牵开器 | Medical instruments - Abdominal retractor type Fritsch |
| DIN 13145-2010 | 医疗器械.塑料锤 | Medical instruments - Mallet of plastic material |
| DIN 13146-2010 | 医疗器械.哈耶克式锤 | Medical instruments - Mallet type Hajek |
| DIN 13147-2010 | 医疗器械.伯格曼式锤 | Medical instruments - Mallet type Bergmann |
| DIN 13148-2010 | 医疗器械.带互换塑料盘的锤 | Medical instruments - Mallet with interchangeable plastic disks |
| DIN 13171-2006 | 医疗器械.Adson-Brown外科组织镊 | Medical instruments - Tissue forceps type Adson-Brown |
| DIN 13172-2006 | 医疗器械.德巴基氏血管镊子 | Medical instruments - Vessel forceps type De Bakey |
| DIN 13173-2005 | 医疗器械.敷料钳 | Medical instruments - Dressing forceps |
| DIN 13174-2005 | 医疗器械.Stieglitz型碎片钳 | Medical instruments - Splinter forceps type Stieglitz |
| DIN 13175-1983 | 医疗器械.扬氏舌钳 | Medical instruments; tongue forceps, type Young |
| DIN 13176-2005 | 医疗器械.器官夹持钳 | Medical instruments - Organ grasping forceps |
| DIN 13177-2005 | 医疗器械.Randall型肾结石钳 | Medical instruments - Kidney stone forceps type Randall |
| DIN 13178-2005 | 医疗器械.Desjardins型胆结石钳 | Medical instruments - Gall stone forceps type Desjardins |
| DIN 13179-2005 | 医疗器械.Vogel型套针夹持钳 | Medical instruments - Trocar holding forceps type Vogel |
| DIN 13180-2005 | 医疗器械.Lahey型甲状腺肿夹持钳 | Medical instruments - Goitre grasping forceps type Lahey |
| DIN 13181-1-1973 | 医疗器械；脑夹用麦肯基氏器械，脑夹使用 | Medical instruments; McKenzie's instruments for brain clips, clips applying |
| DIN 13181-2-1973 | 医疗器械；脑夹用麦肯基器械，脑夹和安装尺寸 | Medical instruments; McKenzie's instruments for brain clips, clips and fitting dimensions |
| DIN 13183-2005 | 医疗器械.Wolff石膏破碎器 | Medical instruments - Plaster breaker Wolff's |
| DIN 13184-2005 | 医疗器械.Farabeuf持骨钳 | Medical instruments - Bone holding forceps Farabeuf's |
| DIN 13185-2005 | 医疗器械.拔指甲钳 | Medical instruments - Onychia forceps |
| DIN 13186-2005 | 医疗器械.Michel夹持钳和拔取钳 | Medical instruments - Clip applying and removing forceps Michel's |
| DIN 13187-2005 | 医疗器械.Semb型持骨钳 | Medical instruments - Bone holding forceps type Semb |
| DIN 13188-2010 | 医疗器械.亨宁式石膏摊开器 | Medical instruments - Plaster cast spreader type Henning |
| DIN 13189-2010 | 医疗器械.费蓝-史密斯-克里封氏椎板切开术钻孔器 | Medical instruments - Laminectomy punches type Ferris-Smith-Kerrison |
| DIN 13190-2005 | 医疗器械.Liston型截骨钳 | Medical instruments - Bone cutting forceps type Liston |
| DIN 13191-2005 | 医疗器械.Stille型咬骨钳 | Medical instruments - Rongeur type Stille |
| DIN 13192-2005 | 医疗器械.Ruskin型咬骨钳 | Medical instruments - Rongeur type Ruskin |
| DIN 13193-2005 | 医疗器械.Luer型咬骨钳 | Medical instruments - Rongeurs type Luer |
| DIN 13194-2005 | 医疗器械.Beyer型咬骨钳 | Medical instruments - Rongeur type Beyer |
| DIN 13195-2005 | 医疗器械.Hartmann型鼻甲切口钳和扁桃体打孔钳 | Medical instruments - Conchotome and tonsil punch forceps type Hartmann |
| DIN 13197-2005 | 医疗器械.Hartmann型鼻和耳息肉钳 | Medical instruments - Nasal and ear polypi forceps type Hartmann |
| DIN 13198-2010 | 医疗器械.高桥式筛状咬骨钳 | Medical instruments - Ethmoid rongeur forceps type Takahashi |
| DIN 13199-2010 | 医疗器械.韦-布二氏和瓦-威二氏筛骨修骨钳 | Medical instruments - Ethmoid rongeur forceps type Weil-Blakesley and Watson-Williams |
| DIN 13411-1999 | 医疗设备中壁墙和仪器的保护.术语和特定数据 | Protection of walls and apparatus in medical facilities - Terms, specific data |
| DIN 13451-2006 | 医疗器械.约瑟夫氏剪刀 | Medical instruments - Scissors type Joseph |
| DIN 13452-2006 | 医疗器械.基尔氏剪刀 | Medical instruments - Scissors type Kilner |
| DIN 13453-2010 | 医疗器械.扁桃体剪 | Medical instruments - Tonsil scissors |
| DIN 13456-2010 | 医疗器械.贝克斯式胆管扩张器 | Medical instruments - Gall duct dilators type Bakes |
| DIN 13457-2010 | 医疗器械.迪特耳式尿道扩张探条和扩张器 | Medical instruments - Urethral bougies and dilating sounds type Dittel |
| DIN 13458-2009 | 医疗器械.结扎针 | Medical instruments - Ligature needle |
| DIN 13459-2008 | 医疗器械.带硬质合金镶件的Stratte型持针器 | Medical instruments - Needle holder type Stratte with carbide inserts |
| DIN 13460-2010 | 医疗器械.希耐瑞式持针器 | Medical instruments - Needle holder type Heaney |
| DIN 13461-2010 | 医疗器械.镶硬质合金的德巴基氏型持针器 | Medical instruments - Neddle holder type De Bakey with carbide inserts |
| DIN 13464-2010 | 医疗器械.舍波尔式牵开器 | Medical instruments - Retractor type Sch?nborn |
| DIN 13465-2010 | 医疗器械.艾德生型止血钳 | Medical instruments - Haemostatic forceps type Adson |
| DIN 13466-2010 | 医疗器械.韦斯特式鼻清理钳 | Medical instruments - Nasal dressing forceps type West |
| DIN 13467-2010 | 医疗器械.马吉尔式麻醉导管导引钳 | Medical instruments - Catheter introducing forceps type Magill |
| DIN 13468-2005 | 医疗器械.Foerster型海绵夹持钳 | Medical instruments - Sponge holding forceps type Foerster |
| DIN 13469-2010 | 医疗器械.艾德生型解剖钳 | Medical instruments - Dissecting forceps type Adson |
| DIN 57753-2-1983 | 心脏手术用电子医疗设备用规则(VDE规范) | Rules relating to intracardiac applications of medical electrical equipment [VDE Guide] |
| DIN 58133-2008 | 医疗压缩袜 | Medical compression hosiery |
| DIN 58230-2010 | 医疗器械.截肢刀 | Medical instruments - Amputation knives |
| DIN 58231-2009 | 医疗器械.Halstead型止血镊 | Medical instruments - Haemostatic forceps type Halstead |
| DIN 58232-2009 | 医疗器械.止血钳.Kocher型和Kocher-Ochsner型止血钳 | Medical instruments - Haemostatic forceps - Kocher and Kocher-Ochsner |
| DIN 58233-2009 | 医疗器械.Overholt-Geissen型止血钳 | Medical instruments - Haemostatic forceps type Overholt-Gei?end?rfer |
| DIN 58234-2009 | 医疗器械.Rochester-Pean型止血钳 | Medical instruments - Hemostatic forceps type Rochester-Pean |
| DIN 58235-1-1983 | 医疗器械.无硬质合金镶件的Mayo-Hegar型持针器 | Medical instruments; needle holder type Mayo-Hegar without carbide inserts |
| DIN 58235-2-2008 | 医疗器械.带硬质合金镶件的Mayo-Hegar型持针器 | Medical instruments - Needle holder type Mayo-Hegar with carbide inserts |
| DIN 58236-1-2010 | 医疗器械.马蒂厄型持针器.第1部分:不镶硬质合金 | Medical instruments - Needle holder type Mathieu - Part 1: Without carbide inserts |
| DIN 58236-2-2010 | 医疗器械.马修式持针器.第2部分:带有镶硬合金齿 | Medical instruments - Needle holder type Mathieu - Part 2: With carbide inserts |
| DIN 58237-2006 | 医疗器械.Feilchenfeld式碎片镊子 | Medical instruments - Splinter forceps type Feilchenfeld |
| DIN 58238-1-2006 | 医疗器械.直式解剖镊子 | Medical instruments - Part 1: Dissection forceps, straight |
| DIN 58238-2-2010 | 医疗器械.解剖钳.第2部分:弯式 | Medical instruments - Dissection forceps - Part 2: Curved |
| DIN 58239-1-2009 | 医疗器械.组织钳子.第1部分:直型 | Medical instruments - Tissue forceps - Part 1: Straight |
| DIN 58239-2-2010 | 医疗器械.组织钳子.第2部分:弯曲(式) | Medical instruments - Tissue forceps - Part 2: Curved |
| DIN 58240-2010 | 医疗器械.以色列式牵开器 | Medical instruments - Retractors type Israel |
| DIN 58241-2009 | 医疗器械.Crile型动脉钳 | Medical instruments - Haemostatic forceps type Crile |
| DIN 58242-2009 | 医疗器械.Dandy型动脉夹 | Medical instruments - Haemostatic forceps type Dandy |
| DIN 58243-2009 | 医疗器械.Kocher型肠钳 | Medical instruments - Intestinal forceps type Kocher |
| DIN 58244-2009 | 医疗器械.Mayo-Robson型肠钳 | Medical instruments - Intestinal forceps type Mayo-Robson |
| DIN 58245-2009 | 医疗器械.backhaus型毛巾夹 | Medical instruments - Towel clamps type Backhaus |
| DIN 58246-2009 | 医疗器械.Mikulicz型腹膜钳 | Medical instruments - Peritoneum forceps type Mikulicz |
| DIN 58247-2010 | 医疗器械.鲁式牵开器 | Medical instruments - Retractors type Roux |
| DIN 58248-2010 | 医疗器械.詹森式牵开器 | Medical instruments - Retractor type Jansen |
| DIN 58249-2010 | 医疗器械.韦特莱纳式牵开器 | Medical instruments - Retractors type Weitlaner |
| DIN 58250-2010 | 医疗器械.手术解剖刀 | Medical instruments - Scalpels |
| DIN 58251-2010 | 医疗器械.贝格曼式解剖刀 | Medical instruments - Scalpels type Bergmann |
| DIN 58252-1-2006 | 医疗器械.不镶硬质合金的直形外科剪刀 | Medical instruments - Part 1: Surgical scissors, straight without carbide inserts |
| DIN 58253-1-2008 | 医疗器械.第1部分:不镶硬质合金的弯形外科剪刀 | Medical instruments - Part 1: Surgical scissors, curved on flat without carbide inserts |
| DIN 58254-2006 | 医疗器械.切口剪刀 | Medical instruments - Scissors for incisions |
| DIN 58255-1-2005 | 医疗器械.Gross 型敷料钳.第1部分:直敷料钳 | Medical instruments - Dressing forceps type Gross - Part 1: Straight |
| DIN 58255-2-2005 | 医疗器械.Gross 型敷料钳.第2部分:弯敷料钳 | Medical instruments - Dressing forceps type Gross - Part 2: Curved |
| DIN 58256-2010 | 医疗器械.托恩尼斯式持针器 | Medical instruments - Needle holder type T?nnis |
| DIN 58257-2010 | 医疗器械.克赖尔型持针器 | Medical instruments - Needle holder type Crile |
| DIN 58259-2010 | 医疗器械.马森式持针器 | Medical instruments - Needle holder type Masson |
| DIN 58260-2008 | 医疗器械.Deschamps型结扎针 | Medical instruments - Ligature needle type Deschamps |
| DIN 58262-2010 | 医疗器械.詹宁斯式张口器 | Medical instruments - Mouth gag type Jennings |
| DIN 58263-2010 | 医疗器械.海斯特型张口器 | Medical instruments - Mouth gag type Heister |
| DIN 58264-2010 | 医疗器械.菲诺切托式肋骨牵开器 | Medical instruments - Rib spreaders type Finochietto |
| DIN 58265-2010 | 医疗器械.菲诺切托式持针器 | Medical instruments - Needle holder type Finochietto |
| DIN 58266-1-2010 | 医疗器械.Crile-Wood式针托.第1部分:无合金刀片 | Medical instruments - Needle holder type Crile-Wood - Part 1: Without carbide inserts |
| DIN 58266-2-2010 | 医疗器械.克利尔-乌德式针托.第2部分:带有合金刀片 | Medical instruments - Needle holder type Crile-Wood - Part 2: With carbide inserts |
| DIN 58267-2010 | 医疗器械.马修式带有内卡爪的持针器 | Medical instruments - Needle holder type Mathieu with inside catch |
| DIN 58270-2006 | 医疗器械.膝弯式镊子 | Medical instruments - Dressing forceps, angular |
| DIN 58271-2006 | 医疗器械.枪状镊子 | Medical instruments - Dressing forceps, bayonet |
| DIN 58272-2009 | 医疗器械.精制显微镜镊子 | Medical instruments - Microscopic forceps, fine pattern |
| DIN 58273-2009 | 医疗器械.固定镊子 | Medical instruments - Fixation forceps |
| DIN 58274-2009 | 医疗器械.虹膜镊子 | Medical instruments - Iris forceps |
| DIN 58275-2008 | 医疗器械.睑板腺囊肿镊子 | Medical instruments - Chalazion forceps |
| DIN 58276-2010 | 医疗器械.艾德生型镊子 | Medical instruments - Forceps type Adson |
| DIN 58277-2006 | 医疗器械；Wachenfeld式缝合回形针用镊子 | Medical instruments - Suture clip applying forceps, type Wachenfeld |
| DIN 58278-2010 | 医疗器械.睫毛镊子 | Medical instruments - Cilia forceps |
| DIN 58279-2006 | 医疗器械.急救箱装剪刀 | Medical instruments - First aid box scissors |
| DIN 58280-2009 | 医疗器械.无硬质合金刀片的的虹膜剪 | Medical instruments - Iris scissors without carbide inserts |
| DIN 58281-1-2006 | 医疗器械.第1部分:不镶硬质合金的斜视用剪刀 | Medical instruments - Part 1: Strabismus scissors without carbide inserts |
| DIN 58282-2006 | 医疗器器械.史蒂文切肢剪刀 | Medical instruments - Tenotomy scissors, type Stevens |
| DIN 58285-2008 | 医疗器械.Volkman 式牵开器 | Medical instruments - Retractor type Volkmann |
| DIN 58286-2010 | 医疗器械.科歇式牵开器 | Medical instruments - Retractor type Kocher |
| DIN 58287-2010 | 医疗器械.克尔特式伤口牵开器 | Medical instruments - Retractor type K?rte |
| DIN 58288-2010 | 医疗器械.兰根贝克式牵开器 | Medical instruments - Retractor type Langenbeck |
| DIN 58289-2010 | 医疗器械.Mikulicz式弯片形腹部和肝脏牵开器 | Medical instruments - Abdominal and liver retractor type Mikulicz, blade curred |
| DIN 58290-2010 | 医疗器械.贝格曼式牵开器 | Medical instruments - Retractor type Bergmann |
| DIN 58291-2010 | 医疗器械.西蒙和马丁式牵开器 | Medical instruments - Retractors type Simon and Martin |
| DIN 58292-2010 | 医疗器械.气管钩 | Medical instruments - Tracheal hook |
| DIN 58293-2008 | 医疗器械.Bose式气管用钩 | Medical instruments - Tracheal hook Bose's |
| DIN 58294-2010 | 医疗器械.代马尔式眼睑牵开器 | Medical instruments - Lid retractor type Desmarres |
| DIN 58295-2010 | 医疗器械.福尔克曼式伤口牵开器 | Medical instruments - Retractor type Volkmann |
| DIN 58296-2008 | 医疗器械.森布刮骨刀 | Medical instruments - Raspatories Semb's |
| DIN 58297-2010 | 医疗器械.杜瓦杨式骨膜剥离器 | Medical instruments - Periosteal raspatories type Doyen |
| DIN 58298-12-1994 | 医疗器械的材料、精加工和检验.第12部分:手锯 | Materials, finish and testing of medical instruments; hand saws |
| DIN 58298-19-2002 | 医疗器械的材料、精加工和测试.第19部分:套管针 | Materials, finish and testing of medical instruments - Part 19: Trocars |
| DIN 58298-20-2003 | 医疗器械的材料、最后加工和测试.第20部分:使用符合DIN 58298-19套针的器械 | Materials, finish and testing of medical instruments - Part 20: Instruments for use with trocars according to DIN 58298-19 |
| DIN 58298-2005 | 医疗器械.材料、精加工和试验 | Medical instruments - Materials, finish and testing |
| DIN 58312-2010 | 医疗器械.肋骨收缩器 | Medical instruments - Rib contractor |
| DIN 58313-2009 | 医疗器械.直型药棉棒 | Medical instruments - Cotton carrier, straight |
| DIN 58314-2008 | 医疗器械.Fein式喉头药棉 | Medical instruments - Throat cotton applicators type Fein |
| DIN 58315-2010 | 医疗器械.库兴型牵开器 | Medical instruments - Retractors type Cushing |
| DIN 58316-2008 | 医疗器械.有延展性的腹部调药刀 | Medical instruments - Abdominal spatulas, malleable |
| DIN 58317-2010 | 医疗器械.汉克式起子 | Medical instruments - Elevator type Henke |
| DIN 58318-2008 | 医疗器械；Langenbeck式分离器 | Medical instruments - Elevators Langenbeck's |
| DIN 58319-2008 | 医疗器械.Williger式手术分离器 | Medical instruments - Elevators Williger |
| DIN 58783-2010 | 医疗器械.布克式耳刮匙 | Medical instruments - Ear curette type Buck |
| DIN 58785-2010 | 医疗器械.哈特曼型窥视镜 | Medical instruments - Ear specula type Hartmann |
| DIN 58788-2010 | 医疗器械.哈特曼-阿累式窥鼻镜 | Medical instruments - Nasal specula type Hartmann-Halle |
| DIN 58794-2010 | 医疗器械.耳镊 | Medical instruments - Ear forceps |
| DIN 58795-2010 | 医疗器械.开口器.滑杆及压舌板的尺寸 | Medical instruments - Mouth gags - Dimensions for slide bars and tongue depressors |
| DIN 58796-2010 | 医疗器械.带手柄的喉镜 | Medical instruments - Laryngeal mirrors with handle |
| DIN 58845-2010 | 医疗器械.霍曼式骨格支杆 | Medical instruments - Bone levers type Hohmann |
| DIN 58846-2010 | 医疗器械.刮骨刀 | Medical instruments - Raspatories |
| DIN 58847-2010 | 医疗器械.韦尔布吕热式骨夹持钳 | Medical instruments - Bone holding forceps type Verbrugge |
| DIN 58849-2-2010 | 医疗器械.可换刀片的手术刀刀柄.刀柄 | Medical instruments - Scalpel handles for detachable blades - Part 2: Handles |
| DIN 58850-2010 | 医疗器械.眼科解剖刀 | Medical instruments - Eye scalpels |
| DIN 58851-2010 | 医疗器械.格雷菲式白内障刀 | Medical instruments - Cataract knives type Graefe |
| DIN 58852-2008 | 医疗器械.探针 | Medical instruments - Probes |
| DIN 58853-2008 | 医疗器械.有孔探针 | Medical instruments - Probes with eye |
| DIN 58854-2010 | 医疗器械.桃金娘叶状探子 | Medical instruments - Myrtle leaf probes |
| DIN 58855-2008 | 医疗器械.Kirschner式有沟探针 | Medical instruments - Director type Kirschner |
| DIN 58856-2010 | 医疗器械.代雅丹式胆结石探针 | Medical instruments - Gall stone probes type Desjardins |
| DIN 58857-2008 | 医疗器械.有沟探针 | Medical instruments - Directors |
| DIN 58858-2008 | 医疗器械.Knig型有沟探针 | Medical instruments - Director type K?nig |
| DIN 58859-2010 | 医疗器械.Tonnis式双端解剖器 | Medical instruments - Dissector type T?nnis, double-ended |
| DIN 58860-2010 | 医疗器械.莱克塞尔式凿子 | Medical instruments - Osteotomes type Lexer |
| DIN 58861-2010 | 医疗器械.兰博特式平面凿子 | Medical instruments - Osteotomes type Lambotte |
| DIN 58862-2010 | 医疗器械.骨刮匙 | Medical instruments - Bone curettes |
| DIN 58863-2010 | 医疗器械.福克曼式刮骨器 | Medical instruments - bone curettes type Volkmann |
| DIN 58864-2010 | 医疗器械.西蒙,施罗德及哈雷式刮骨器 | Medical instruments - Bone curettes type Simon, type Schr?der and type Halle |
| DIN 58865-1988 | 医疗器械.兰根贝克式切除手术刀 | Medical instruments; resection knives type Langenbeck |
| DIN 58866-2010 | 医疗器械.巴氏鼻中隔刀 | Medical instruments - Septum knives type Ballenger |
| DIN 58867-2010 | 医疗器械.Breunings式隔膜手术刀 | Medical instruments - Septum knife type Brünings |
| DIN 58940-1-2002 | 医疗微生物学.病原细菌对杀菌剂敏感性的测定方法.第1部分:术语 | Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 1: Terminology |
| DIN 58940-2 Bb.2-2002 | 医疗微生物学.病原细菌对杀菌剂敏感性的检测.第2部分:细菌培养基传播试验用活性物质传递体:绘制标准曲线用 | Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 2: Active substance carriers for the agar diffusion test; Carrier loads and values required for drawing a standard curve |
| DIN 58940-20-2002 | 医疗微生物学.病原细菌对杀菌剂敏感性的检测.第20部分:杀菌剂的编码 | Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 20: Codes for antimicrobial agents |
| DIN 58940-4-2002 | 医疗微生物学.病源细菌对杀菌剂敏感性的检测.第4部分:最小抑制浓度的评价等级 | Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 4: Evaluation classes of the minimum inhibitory concentration |
| DIN 58940-8-2002 | 医疗微生物学.病原细菌对杀菌剂敏感性的测定方法.第8部分:微量稀释:一般方法和特殊要求 | Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 8: Microdilution; General method-specific requirements |
| DIN 58940-82-2002 | 医疗微生物学.微生物病源细菌对杀菌剂敏感性的检测.第82部分:微量稀释.难养细菌试验的特殊要求 | Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 82: Microdilution; Special requirements for testing of fastidious bacteria |
| DIN 58940-83-2002 | 医疗微生物学.微生物病源细菌对杀菌剂敏感性的检测.第83部分:微量稀释.严格控制的厌气细菌试验用特殊要求 | Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 83: Microdilution; Special requirements for testing of strictly anaerobically bacteria |
| DIN 58940-84-2002 | 医疗用微生物学.微生物病源细菌对杀菌剂敏感性的检测.第84部分:微量稀释.耐抗菌剂的真菌试验的特殊要求 | Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 84: Microdilution; Special requirements for testing of fungi against antifungal agents |
| DIN 58953-6-2010 | 消毒.消毒材料供应.第6部分:欲灭菌医疗器械用包装材料的微生物障阻检验 | Sterilization - Sterile supply - Part 6: Microbial barrier testing of packaging materials for medical devices which are to be sterilized |
| DIN 58953-8-2010 | 消毒.消毒材料供应.第8部分:无菌医疗装置的输给系统 | Sterilization - Sterile supply - Part 8: Logistics of sterile medical devices |
| DIN 58955-1-2003 | 医疗用净化设备.第1部分:术语 | Decontamination equipment for medical use - Part 1: Terminology |
| DIN 58959 Bb.1-1997 | 医疗微生物学质量管理.综述和索引 | Quality management in medical microbiology - Overview and index |
| DIN 58959-1-1997 | 医疗微生物学质量管理.第1部分:质量管理(QM)体系要求 | Quality management in medical microbiology - Part 1: Requirements for the QM system |
| DIN 58959-10 Bb.1-1997 | 医疗微生物学质量管理.第10部分:试剂、着色剂、生物材料检验用对照菌株要求.常用材料用对照菌株 | Quality management in medical microbiology - Part 10: Requirements for the use of control strains for testing reagents, dyes and biological materials; control strains for commonly used materials |
| DIN 58959-10-1997 | 医疗微生物学质量管理.第10部分:试剂、色素和生物材料检验用对照菌株要求 | Quality management in medical microbiology - Part 10: Requirements for the use of control strains for testing reagents, dyes and biological materials |
| DIN 58959-11-1997 | 医疗微生物学质量管理.第11部分:检测可供使用的试验和试验工具箱用对照菌株要求 | Quality management in medical microbiology - Part 11: Requirements for the use of control material for testing ready-to-use tests and test kits |
| DIN 58959-12 Bb.1-1997 | 医疗微生物学质量管理.第12部分:免疫研究系统检验对照菌株要求.常用免疫诊断用对照菌株 | Quality management in medical microbiology - Part 12: Requirements for the use of control material for testing immunological reagent kits; control material for commonly used immune diagnostics |
| DIN 58959-12-1997 | 医疗微生物学质量管理.第12部分:免疫检查系统检验用对照菌株要求 | Quality management in medical microbiology - Part 12: Requirements for the use of control material for testing immunological reagent kits |
| DIN 58959-14-1997 | 医疗微生物学质量管理.第14部分:需氧菌敏感性检验对照菌株要求 | Quality management in medical microbiology - Part 14: Requirements for the use of control strains for susceptibility testing of aerobic bacteria |
| DIN 58959-15 Bb.1-1997 | 医疗微生物学质量管理.第15部分:厌氧病原体敏感性检验对照菌株要求.厌氧菌用MHK-极限(控制)区 | Quality management in medical microbiology - Part 15: Requirements for the use of control strains for susceptibility testing of anaerobic bacteria; MIC/IZD limits for anaerobes |
| DIN 58959-16-1997 | 医疗微生物学质量管理.第16部分:特种细菌敏感性检验对照菌株要求 | Quality management in medical microbiology - Part 16: Requirements for the use of control strains for susceptibility testing of special bacteria |
| DIN 58959-17-1997 | 医疗微生物学质量管理.第17部分:分支杆菌属研究对照菌株要求 | Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria |
| DIN 58959-18 Bb.1-1997 | 医疗微生物学质量管理.第18部分:支原菌属研究对照菌株要求.常用培养基和试剂对照菌株 | Quality management in medical microbiology - Part 18: Requirements for the use of control strains for the examination of mycoplasms; control strains for commonly used culture media and reagents |
| DIN 58959-18-1997 | 医疗微生物学质量管理.第18部分:支原菌属研究对照菌株要求 | Quality management in medical microbiology - Part 18: Requirements for the use of control strains for the examination of mycoplasms |
| DIN 58959-19 Bb.1-1997 | 医疗微生物学质量管理.第19部分:真菌研究对照菌株要求.常用培养基和试剂对照菌株 | Quality management in medical microbiology - Part 19: Requirements for the use of control strains for the examination of fungi; control strains for commonly used culture media and reagents |
| DIN 58959-19-1997 | 医疗微生物学质量管理.第19部分:真菌研究对照菌株要求 | Quality management in medical microbiology - Part 19: Requirements for the use of control strains for the examination of fungi |
| DIN 58959-2 Bb.1-1997 | 医疗微生物学质量管理.第2部分:试样采集、运输及验收要求.专用试样特性 | Quality management in medical microbiology - Part 2: Requirements for sample collection, transport and acception of specimens; characteristics for special specimens |
| DIN 58959-2-1997 | 医疗微生物学质量管理.第2部分:试样采集、运输和验收要求 | Quality management in medical microbiology - Part 2: Requirements for sample collection, transport and acceptance of specimens |
| DIN 58959-20-1997 | 医疗微生物学质量管理.第20部分:原虫和较高的有机微生物研究对照菌株要求 | Quality management in medical microbiology - Part 20: Requirements for the use of control material for the examination of protozoae and microorganisms of higher order |
| DIN 58959-3-1997 | 医疗微生物学质量管理.第3部分:申请表和报告单要求 | Quality management in medical microbiology - Part 3: Requirements for request and report forms |
| DIN 58959-4-1997 | 医疗微生物学质量管理.第4部分:光学显微镜测试要求 | Quality management in medical microbiology - Part 4: Requirements for investigations using light microscopes |
| DIN 58959-6 Bb.1-1997 | 医疗微生物学质量管理.第6部分:对照菌株要求.菌株培养和应用培养细菌的生产和保管实例 | Quality management in medical microbiology - Part 6: Requirements for control strains; examples for production and preservation of bacteria used as stock cultures and working cultures |
| DIN 58959-6 Bb.2-1997 | 医疗微生物学质量管理.第6部分:对照菌株要求.菌株培养和应用培养的真菌的生产和保管实例 | Quality management in medical microbiology - Part 6: Requirements for control strains; examples for production and preservation of fungi used as stock cultures and working cultures |
| DIN 58959-6-1997 | 医疗微生物学质量管理.第6部分:对照菌株要求 | Quality management in medical microbiology - Part 6: Requirements for control strains |
| DIN 58959-7 Bb.1-1997 | 医疗微生物学质量管理.第7部分:使用对照菌株的一般要求.对照菌株供应源 | Quality management in medical microbiology - Part 7: General requirements for the use of control strains; sources of supply for control strains |
| DIN 58959-7 Bb.2-1997 | 医疗微生物学质量管理.第7部分:使用对照菌株的一般要求.常用对照菌株的ATTC编号和DSM编号 | Quality management in medical microbiology - Part 7: General requirements for the use of control strains; ATTC and DSM numbers of commonly used control strains |
| DIN 58959-7 Bb.3-1997 | 医疗微生物学质量管理.第7部分:使用对照菌株的一般要求.试验结果文件对照卡实例 | Quality management in medical microbiology - Part 7: General requirements for the use of control strains; examples for control cards documentation of test results |
| DIN 58959-7-1997 | 医疗微生物学质量管理.第7部分:使用对照菌株的一般要求 | Quality management in medical microbiology - Part 7: General requirements for the use of control strains |
| DIN 58959-8-1997 | 医疗微生物学质量管理.第8部分:涂抹棉签、运输介质、浸渍介质和血液培养介质检验对照菌株要求 | Quality management in medical microbiology - Part 8: Requirements for the use of control strains for testing swabs, transport media, media of dip-slides, and blood culture media |
| DIN 58959-9 Bb.1-1997 | 医疗微生物学质量管理.第9部分:培养基检验对照菌株要求.常用培养基对照菌株 | Quality management in medical microbiology - Part 9: Requirements for the use of control strains for testing culture media; control strains for commonly used culture media |
| DIN 58959-9 Bb.2-1997 | 医疗微生物学质量管理.第9部分:培养基检验用对照菌株要求.随时可用的培养基最长保存时间 | Quality management in medical microbiology - Part 9: Requirements for the use of control strains for testing culture media; maximum storage times for ready to use culture media |
| DIN 58959-9-1997 | 医疗微生物学质量管理.第9部分:培养基检验对照菌株要求 | Quality management in medical microbiology - Part 9: Requirements for the use of control strains for testing culture media |
| DIN 58962-1-1994 | 医疗微生物学.下呼吸道感染诊断.第1部分:术语、一般要求 | Medical microbiology - Diagnosis of infections of the lower respiratory tract (LRT) - Part 1: Terminology, general requirements |
| DIN 58962-2-1994 | 医疗微生物学.下呼吸道感染诊断.第2部分:显微诊察 | Medical microbiology - Diagnosis of infections of the lower respiratory tract (LRT) - Part 2: Microscopic examination |
| DIN 58962-3-1996 | 医疗微生物学.下呼吸道感染诊断.第3部分:细菌和真菌培养化验 | Medical microbiology - Diagnosis of infections of the lower respiratory tract - Part 3: Cultural examination for the detection of bacteria and fungi |
| DIN 6814-6-2009 | 放射技术领域中的术语 第6部分:医疗中使用X放射进行诊断 | Terms in the field of radiological technique - Part 6: Diagnostic use of X-radiation in medicine |
| DIN 6815 Berichtigung 1-2005 | 300kV及以下的医疗X射线设备.安装、维修和必要修改后辐射防护的检验规则 | Medical X-ray equipment up to 300 kV - Rules for testing of radiation protection after installation, maintenance and essential modification, Corrigenda to DIN 6815:2005-05 |
| DIN 6815-2005 | 300kV及以下的医疗X射线设备.安装、维修和必要修改后辐射防护的检验规则 | Medical X-ray equipment up to 300 kV - Rules for testing of radiation protection after installation, maintenance and essential modification |
| DIN 6843-2006 | 搬运医疗设备中未密封的放射性材料的射线防护规则 | Radiation protection rules for handling of unsealed radioactive material in medicine |
| DIN 6844-1-2005 | 核医疗部门.第1部分:非密封放射源的诊断应用装置和设备的规则 | Nuclear medicine departments - Part 1: Rules for the installation and equipment for diagnostic applications of unsealed radioactive sources |
| DIN 6844-2-2005 | 核医疗部门.第2部分:非密封放射源的治疗应用装置和设备的规则 | Nuclear medicine departments - Part 2: Rules for the installation and equipment for therapeutic applications of unsealed radioactive sources |
| DIN 6844-3-2006 | 核医疗部门.第3部分:辐射防护计算 | Nuclear medicine departments - Part 3: Radiation protection calculations |
| DIN 6847-2-2008 | 医疗电子加速器.第2部分:结构辐射防护的构造规则 | Medical electron accelerators - Part 2: Rules for construction of structural radiation protection |
| DIN 6850-2006 | 核医疗用的射线防护箱、防护桌和防护柜.要求和分类 | Radiation protection containers, tables and safes for use in nuclear medicine - Requirements and classification |
| DIN 6853-5-1992 | 医疗遥控自动驱动后装载系统.稳定性检验 | Medical remote-controlled automatically-driven afterloading systems; constancy testing |
| DIN 6855-1-2009 | 核医疗测量系统的恒定性试验.第1部分:体内和体外测量用辐射计数系统(IEC/TR 61948-1:2001,修改件) | Constancy testing of nuclear medical measuring systems - Part 1: Radiation counting systems for measurements in vivo and in vitro (IEC/TR 61948-1:2001, modified) |
| DIN 6855-11-2009 | 核医疗学器械的稳定性测试 第11部分:放射性核校准器(修改的IEC/TR 61948-4-2006) | Constancy testing of nuclear medicine instruments - Part 11: Radionuclide calibrators (IEC/TR 61948-4:2006, modified) |
| DIN 6855-2-2005 | 核医疗仪器的质量控制.第2部分:用于单光子X线断层术的带旋转检测头的角型γ射线摄像机和平面闪烁扫描术的单 | Quality control of nuclear medicine instruments - Part 2: Constancy testing of single crystal gamma-camers used in planar scintigraphy and in anger type gamma cameras with rotating detector heads used in single photon emission tomography |
| DIN 6855-4-2004 | 核医疗测量系统的质量检验.第4部分:正电子放射X线体层照片的稳定性试验 | Quality control of nuclear medicine instruments - Part 4: Constancy testing of positron emission tomographs (PET) |
| DIN 6856-1-2007 | 放射学底片影视箱和观察条件.第1部分:医疗诊断中质量保证的要求和测量 | Radiological film viewing boxes and viewing conditions - Part 1: Requirements and measures of quality assurance in medical diagnostics |
| DIN 6862-1-1992 | 医疗诊断中X射线图相的识别和表征.直接和间接X线照相术 | Identification and characterisation of radiological images in medical diagnosis; direct and indirect radiography |
| DIN 6867-10-1995 | 医疗X光照相用屏蔽胶片系统的感光度.第10部分:速度和平均梯度的额定值 | Sensitometry of screen-film systems for medical radiography - Part 10: Nominal values of speed and average gradient |
| DIN 6867-3-2000 | 医疗X射线照相用软片系列的感光测定.第3部分:乳腺X射线摄相感光曲线形状、速度和平均梯度的测定方法 | Sensitometry of screen-film systems for medical radiography - Part 3: Method for determination of sensitometric curve shape, speed and average gradient for mammography |
| DIN 6868-4-2007 | 诊断X射线部门的图像质量保证.第4部分:荧光检查用医疗X射线设备的稳定性测试 | Image quality assurance in diagnostic X-ray departments - Part 4: Constancy testing of medical X-ray equipment for fluoroscopy |
| DIN 6870-1-2009 | 医疗放射学的质量管理体系.第1部分:放射线疗法 | Quality management system in medical radiology - Part 1: Radiotherapy |
| DIN 6878-1-1998 | 医疗放射图像的数字存储.第1部分:图像数字存储一般要求 | Digital archiving in medical radiology - Part 1: General requirements for the archiving of images |
| DIN 96010-2009 | 医疗器械.van Buren型腐骨钳 | Medical instruments - Sequestrum forceps type van Buren |
| DIN 96012-2009 | 医疗器械.Olivecrona型外科剪刀 | Medical instruments - Surgical scissors type Olivecrona |
| DIN 96015-2009 | 医疗器械.Stille型石膏剪 | Medical instruments - Plaster scissors type Stille |
| DIN 96016-2009 | 医疗器械.Dahlgreen型截骨钳 | Medical instruments - Bone cutting forceps type Dahlgreen |
| DIN 96020-2009 | 医疗器械.Sauerbruch型裂口剪刀 | Medical instruments - Rip shears type Sauerbruch |
| DIN 96022-2009 | 医疗器械.Citelli式骨钳 | Medical instruments - Bone forceps type Citelli |
| DIN 96023-2009 | 医疗器械.医用筛形咬骨钳Brünings式镊子 | Medical instruments - Ethmoid rangeur forceps type Brünings |
| DIN 96024-2009 | 医疗器械.耶克-克劳斯(Hajek-Claus)式筛形咬骨钳 | Medical instruments - Ethmoid rongeur forceps type Hajek-Claus |
| DIN 96025-2009 | 医疗器械.Craig式筛形修骨钳子 | Medical instruments - Ethmoid rongeur forceps type Craig |
| DIN 96028-2009 | 医疗器械.医用Dieffenbach式止血镊子 | Medical instruments - Haemostatic forceps type Dieffenbach |
| DIN 96031-2009 | 医疗器械.Guyon式止血钳 | Medical instruments - Haemostatic forceps type Guyon |
| DIN 96033-2009 | 医疗器械.特海姆-卡伦(Wertheim-Cullen)式止血钳 | Medical instruments - Haemostatic forceps type Wertheim-Cullen |
| DIN 96035-2009 | 医疗器械.Semb式止血钳 | Medical instruments - Haemostatic forceps type Semb |
| DIN 96036-2009 | 医疗器械.Price-Thomas式止血钳 | Medical instruments - Haemostatic forceps type Price-Thomas |
| DIN 96053-2009 | 医疗器械.Ollier式牵开器 | Medical instruments - Retractor type Ollier |
| DIN 96056-2009 | 医疗器械.骨锉 | Medical instruments - Bone raspatory |
| DIN 96057-2009 | 医疗器械.Sedillot式骨锉 | Medical instruments - Raspatory type Sedillot |
| DIN 96058-2009 | 医疗器械.兰格-霍曼(Lange-Hohmann)式起子和骨折复位挺子 | Medical instruments - Elevator and bone lever type Lange-Hohmann |
| DIN 96060-2009 | 医疗器械.Langenbeck式起子 | Medical instruments - Elevator type Langenbeck |
| DIN 96062-2009 | 医疗器械.Rollet式泪腺囊牵开器 | Medical instruments - Lachrymal sac retractor type Rollet |
| DIN 96063-2009 | 医疗器械.库欣（Cushing）式神经拉钩 | Medical instruments - Nerve hook type Cushing |
| DIN 96064-2009 | 医疗器械.Tonnis式硬脑膜钩 | Medical instruments - Dura hook type T?nnis |
| DIN 96065-2009 | 医疗器械.Graefe式虹膜钩 | Medical instruments - Iris hook type Graefe |
| DIN 96066-2009 | 医疗器械.Graefe式斜视钩 | Medical instruments - Strabismus hook type Graefe |
| DIN 96067-2009 | 医疗器械.Lucae式耳钩 | Medical instruments - Ear hook type Lucae |
| DIN 96071-2009 | 医疗器械.Olivecrona式头部压舌板 | Medical instruments - Brain spatula type Olivecrona |
| DIN 96073-2009 | 医疗器械.双面压舌钳 | Medical instruments - Tongue depressor, double-ended |
| DIN CEN/TS 14796-2004 | 医疗信息学.数据类型 | Health informatics - Data types; German version CEN/TS 14796:2004, text English |
| DIN CWA 14446-2002 | 欧洲通用物品记录器.EGAR、工作方法和医疗保健部门中的投标和采购工艺相关的概念性描述 | European Generic Article Register - Conceptual description of EGAR, working methodology and relation to the tendering and procurement process in the healthcare sector; English version CWA 14446:2002 |
| DIN EN 1041-2008 | 由医疗装置制造商提供的信息 | Information supplied by the manufacturer of medical devices; German version EN 1041:2008 |
| DIN EN 12322-1999 | 体外诊断医疗装置.微生物用培养基.培养基的功能标准 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media; German version EN 12322:1999 |
| DIN EN 12376-1999 | 体外诊断用医疗器械.由厂商提供的生物着色用活体外诊断试剂信息; 德文版本 EN 12376:1999 | In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology; German version EN 12376:1999 |
| DIN EN 12435-2006 | 医疗信息学.健康科学测量结果表达式 | Health Informatics - Expression of results of measurements in health sciences; English version EN 12435:2006 |
| DIN EN 12967-2-2008 | 医疗信息学.服务体系机构.第2部分:信息综述 | Health informatics - Service architecture - Part 2: Information viewpoint; English version EN 12967-2:2007 |
| DIN EN 12967-3-2008 | 医疗信息学.服务体系机构.第3部分:计算观点 | Health informatics - Service architecture - Part 3: Computational viewpoint; English version EN 12967-3:2007 |
| DIN EN 13532-2002 | 自测用体外诊断用医疗装置的一般要求 | General requirements for in vitro diagnostic medical devices for self-testing; German version EN 13532:2002, German and English texts |
| DIN EN 13609-1-2005 | 健康信息学.医疗保健系统基础信息维护用信息.第1部分:编码表的更新 | Health Informatics - Messages for maintenance of supporting information in healthcare systems - Part 1: Updating of coding schemes; English version EN 13609-1:2005 |
| DIN EN 13612-2002 | 体外诊断医疗装置的性能评价 | Performance evaluation of in vitro diagnostic medical devices; German version EN 13612:2002, German and English texts |
| DIN EN 13624-2004 | 化学消毒剂和抗菌剂.医疗器械用消毒剂的杀菌活性评定用定量悬浮试验.试验方法和要求(第2阶段第1步) | Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1); German version EN 13624:2003 |
| DIN EN 13718-1-2008 | 医疗交通工具及其设备.空中救护机.第1部分:空中救护机用医疗装置的要求 | Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances; English version of DIN EN 13718-1:2008-11 |
| DIN EN 13726-3-2003 | 非活动性医疗器械.伤口主要敷料试验方法.第3部分:防水性 | Non-active medical devices - Test methods for primary wound dressings - Part 3: Waterproofness; German version EN 13726-3:2003 |
| DIN EN 13726-4-2003 | 非活动性医疗器械.伤口主要敷料试验方法.第4部:一致性 | Non-active medical devices - Test methods for primary wound dressings - Part 4: Conformability; German version EN 13726-4:2003 |
| DIN EN 13726-6-2003 | 非活动性医疗器械.伤口主要敷料试验方法.第6部分:气味控制 | Non-active medical devices - Test methods for primary wound dressings - Part 6: Odour control; German version EN 13726-6:2003 |
| DIN EN 13727-2004 | 化学消毒剂和防腐剂.医疗器械用化学消毒剂的杀菌作用评价用定量悬浮试验.试验方法和要求(第2阶段第1步) | Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1); German version EN 13727:2003 |
| DIN EN 13795-1-2009 | 作为医务用品的病人,医疗人员和医用设备用手术盖单,长外衣和无污染套装.第1部分:厂商,加工者和产品的一般要 | Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Part 1: General requirements for manufacturers, processors and products(includes Amendment A1:2009); English version of DIN EN 13795-1:2009-10 |
| DIN EN 13795-2-2009 | 用作医疗器械的患者,医护人员和医疗器械用覆盖巾,手术服和清洁空气套装.第2部分:试验方法,德文版本EN 13795 | Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 2: Test methods ; German version EN 13795-2:2004+A1:2009 |
| DIN EN 13795-3-2009 | 患者、临床医务人员和医疗设备作为医疗器材使用的手术用布帘、睡衣、超净套装.第3部分:性能要求和性能水平. | Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 3: Performance requirements and performance levels (includes Amendment A1:2009); English version of DIN EN 13795-3:2009-12 |
| DIN EN 13824-2005 | 医疗装置的消毒.液体医疗装置的无菌处理.要求 | Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements; German version EN 13824:2004 |
| DIN EN 13940-1-2007 | 医疗信息学.医护保障连续性的概念系统.第一部分:基本概念 | Health informatics - System of concepts to support continuity of care - Part 1: Basic concepts; English version EN 13940-1:2007 |
| DIN EN 13975-2003 | 体外诊断用医疗装置的验收试验用取样规程.统计特性 | Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects; German version EN 13975:2003, German and English texts |
| DIN EN 14079-2003 | 非放射性医疗装置.绷带纱布、脱脂棉和粘胶纱布的性能要求和试验方法 | Non-active medical devices - Performance requirements and test methods for absorbent cotton gauze and absorbent cotton and viscose gauze; German version EN 14079:2003 |
| DIN EN 14254-2004 | 体外诊断医疗装置.收集来自于人体的试样(血液除外)用一次性容器 | In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans; German version EN 14254:2004 |
| DIN EN 14463-2008 | 医学信息学.描述医疗分类系统内容的术语.分类标记语言 | Health informatics - A syntax to represent the content of medical classification systems - ClaML; English version EN 14463:2007 |
| DIN EN 14484-2004 | 医疗信息.EU数据保护指令包含的个人医疗数据的国际传送.高级安全政策 | Health informatics - International transfer of personal health data covered by the EU data protection directive - High level security policy; German version EN 14484:2003, text in English |
| DIN EN 14485-2004 | 医疗信息.EU数据保护指令中包含的国际应用中个人医疗数据处理指南 | Health informatics - Guidance for handling personal health data in international applications in the context of the EU data protection directive; German version EN 14485:2003, text in English |
| DIN EN 14563-2009 | 化学消毒剂和防腐剂.医疗领域中器械用化学消毒剂的分枝杆菌或杀结核菌活性评估用定量带菌体试验.试验方法和 | Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2);English version of DIN EN 14563:2009-02 |
| DIN EN 15424-2007 | 医疗设备灭菌.低温蒸汽和甲醛.医疗设备灭菌过程的制定、确认和常规控制的要求 | Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices; English version of DIN EN 15424:2007-08 |
| DIN EN 1639-2010 | 牙科学.牙科用医疗器械.仪器.德文版本 EN 1639-2009 | Dentistry - Medical devices for dentistry - Instruments; German version EN 1639:2009 |
| DIN EN 1641-2010 | 牙科学.牙科用医疗器械.材料.德文版本EN 1641-2009 | Dentistry - Medical devices for dentistry - Materials; German version EN 1641:2009 |
| DIN EN 1642-2010 | 牙科学.牙科用医疗器械.牙科植入物.德文版本EN 1642-2009 | Dentistry - Medical devices for dentistry - Dental implants; German version EN 1642:2009 |
| DIN EN 1707-1997 | 注射器,套管针和其他医疗器械带6%锥度(吕埃尔)的圆锥连接件.可闩紧的圆锥连接件 | Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings; German version EN 1707:1996 |
| DIN EN 1789-2007 | 医疗车辆及其设备.道路救护车 | Medical vehicles and their equipment - Road ambulances; English version of DIN EN 1789:2007-08 |
| DIN EN 300674-1-2005 | 电磁兼容性和无线电频谱情况(ERM).道路运输和交通的远程信息技术(RTTT).在5.8 GHz-ISM(工业、科学和医疗)频 | Electromagnetic compatibility and Radio spectrum Matters (ERM) - Road Transport and Traffic Telematics (RTTT) - Dedicated Short Range Communication (DSRC) transmission equipment (500 kbit/s/250 kbit/s) operating in the 5,8 GHz Industrial, Scientific and Medical (ISM) band - Part 1: General characteristics and test methods for Road Side Units (RSU) and On-Board Units (OBU) (Endorsement of the English version EN 300674-1 V1.2.1 (2004-08) as German standard) |
| DIN EN 300674-2-1-2005 | 电磁兼容性和无线电频谱情况(ERM).道路运输和交通的远程信息技术(RTTT).在5.8 GHz-ISM(工业、科学和医疗)频 | Electromagnetic compatibility and Radio spectrum Matters (ERM) - Road Transport and Traffic Telematics (RTTT) - Dedicated Short Range Communication (DSRC) transmission equipment (500 kbit/s/250 kbit/s) operating in the 5,8 GHz Industrial, Scientific and Medical (ISM) band - Part 2: Harmonized EN under article 3.2 of the R&TTE Directive - Sub-part 1: Requirements for the Road Side Units (RSU) (Endorsement of the English version EN 300674-2-1 V1.1.1 (2004-08) as German standard) |
| DIN EN 300674-2-2-2005 | 电磁兼容性和无线电频谱情况(ERM).道路运输和交通的远程信息技术(RTTT).在5.8 GHz-ISM(工业、科学和医疗)频 | Electromagnetic compatibility and Radio spectrum Matters (ERM) - Road Transport and Traffic Telematics (RTTT) - Dedicated Short Range Communication (DSRC) transmission equipment (500 kbit/s/250 kbit/s) operating in the 5,8 GHz Industrial, Scientific and Medical (ISM) band - Part 2: Harmonized EN under article 3.2 of the R&TTE Directive - Sub-part 2: Requirements for the On-Board Unit (OBU) (Endorsement of the English version EN 300674-2-2 V1.1.1 (2004-08) as German standard) |
| DIN EN 301839-1-2010 | 电磁兼容性和无线频谱管理(ERM).短距离装置(SRD).工作频率范围为402MHz～405MHz的超低功率有源医疗植入物(U | Electromagnetic compatibility and Radio spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz - Part 1: Technical characteristics and test methods (Endorsement of the English version EN 301839-1 V1.3.1 (2009-10) as German standard) |
| DIN EN 301839-2-2010 | 电磁兼容性和无线频谱管理(ERM).短距离装置(SRD).工作频率范围为402MHz～405MHz的超低功率有源医疗植入物(U | Electromagnetic compatibility and Radio spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz - Part 2: Harmonized EN covering the essential requirements of article 3.2 of the R&TTE Directive (Endorsement of the English version EN 301839-2 V1.3.1 (2009-10) as German standard) |
| DIN EN 302537-2-2008 | 电磁兼容性和无线电频谱管理(ERM).短程无线电设备(SRD).使用频率范围401MHz～402MHz和405MHz～406 MHz的超 | Electromagnetic compatibility and Radio Spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Medical Data Service Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz - Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive (Endorsement of the English version EN 302537-2 V1.1.2 (2007-12) as German standard) |
| DIN EN 45502-1-1998 | 活性可植入医疗装置.第1部分:安全性、标识和由制造商提供的信息的一般要求 | Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer; German version EN 45502-1:1997 |
| DIN EN 45502-2-1-2004 | 活性可植入的医疗装置.第2-1部分:用于治疗缓慢性心率失常的活性可植入医疗装置(心脏起搏器)的特殊要求 | Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers); German version EN 45502-2-1:2003 |
| DIN EN 45502-2-2 Berichtigung 1-2009 | 可植入式医疗器械.第2-2部分:用于治疗缓慢性心率失常的活性可植入医疗器件的特殊要求(心脏起搏器),德文版本 | Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators); German version EN 45502-2-2:2008, Corrigendum to DIN EN 45502-2-2 (VDE 0750-10-2):2008-10; German version CENELEC-Cor.:2009 to EN 45502-2-2:2008 |
| DIN EN 45502-2-2-2008 | 有源可植入的医疗装置.第2-2部分:用于治疗缓慢性心率失常的有源可植入医疗装置(包括可植入心脏起搏器)的特 | Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators); German version EN 45502-2-2:2008 |
| DIN EN 55011 Bb.1-1999 | 工业,科学和医疗设备(ISM设备).国际电信联盟(ITU)规定的频带内发射水平的指南 | Industrial, scientific and medical equipment (ISM) - Guidelines for emission levels within the bands designated by the ITU (IEC/CISPR 28:1997) |
| DIN EN 55011-2010 | 工业、科学和医疗设备.射频干扰特性.极限值和测量方法(IEC/CISPR 11-2009,修改的).德文版本 EN 55011-2009 | Industrial, scientific and medical equipment - Radio-frequency disturbance characteristics - Limits and methods of measurement (IEC/CISPR 11:2009, modified); German version EN 55011:2009 |
| DIN EN 556-1 Berichtigung 1-2006 | 医疗设施的消毒.对标有"消毒"字样医疗设施要求.第1部分:最终消毒医用的要求 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001, Corrigenda to DIN EN 556-1:2002-03; German version EN 556-1:2001/AC:2006 |
| DIN EN 556-1-2002 | 医疗设备消毒.标有"消毒"字样医疗设备要求.第1部分:定期消毒医疗设备要求 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001 |
| DIN EN 556-2-2004 | 医疗器械的消毒.标有"消毒"字样的医疗器械的要求.第2部分:经无菌处理的医疗器械的要求 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices; German version EN 556-2:2003 |
| DIN EN 60598-2-25-2005 | 灯具.第2-25部分:特殊要求.医院和医疗保健中心临床区域用灯具 | Luminaires - Part 2-25: Particular requirements - Luminaires for use in clinical areas of hospitals and health care buildings (IEC 60598-2-25:1994 + Corrigendum 1994 + A1:2004); German version EN 60598-2-25:1994 + A1:2004 |
| DIN EN 60601-1 Bb.2-2009 | 医疗实践中电气设备用图形符号 | Graphical symbols for electrical equipment in medical practice (IEC/TR 60878:2003, modified), Text in German and English |
| DIN EN 60601-1 Berichtigung 1-2008 | 医疗电气设备.第1部分:基本安全和重要性能的一般要求.技术勘误DIN EN 60601-1(VDE 0750-1)-2007 | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005); German version EN 60601-1:2006, Corrigendum to DIN EN 60601-1 (VDE 0750-1):2007-07 |
| DIN EN 60601-1-10-2008 | 医疗电气设备.第1-10部分:基本安全和重要性能的通用要求.附属标准:理疗闭环控制器的开发要求 | Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers (IEC 60601-1-10:2007); German version EN 60601-1-10:2008 |
| DIN EN 60601-1-3 Berichtigung 1-2010 | 医疗电气设备.第1-3部分:基本安全和重要性能的一般要求.附属标准:诊断X射线设备中辐射防护 (IEC 60601-1-3- | Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment (IEC 60601-1-3:2008); German version EN 60601-1-3:2008, Corrigendum to DIN EN 60601-1-3 (VDE 0750-1-3):2008-12; German version CENELEC-Cor. :2010 to EN 60601-1-3:2008 |
| DIN EN 60601-1-3-2008 | 医疗电气设备.第1-3部分:基本安全和重要性能的通用标准.附属标准:X射线诊断设备中的辐射防护(IEC 60601-1-3 | Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment (IEC 60601-1-3:2008); German version EN 60601-1-3:2008 |
| DIN EN 60601-1-4-2001 | 医疗电气设备.第1-4部分:安全性一般要求.补充标准:可编程电气医疗系统 | Medical electrical equipment - Part 1-4: General requirements for safety; Collateral standard: Programmable electrical medical systems (IEC 60601-1-4:1996 + A1:1999); German version EN 60601-1-4:1996 + A1:1999 |
| DIN EN 60601-1-8 Berichtigung 1-2010 | 医用电气设备.第1-8部分:基本安全和基本性能用通用要求.汇编标准:在医疗电气设备和医疗电气系统中警报系统 | Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (IEC 60601-1-8:2006); German version EN 60601-1-8:2007, Corrigendum to DIN EN 60601-1-8 (VDE 0750-1-8):2008-02; German version CENELEC-Cor. :2010 to EN 60601-1-8:2007 |
| DIN EN 60601-1-8-2008 | 医用电气设备.第1-8部分:基本安全和基本性能通用要求.汇编标准:医疗电气设备和医疗电气系统中警报系统的一 | Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (IEC 60601-1-8:2006); German version EN 60601-1-8:2007 |
| DIN EN 60601-1-9-2008 | 医疗电气设备.第1-9部分:基本安全和重要性能的通用要求.附属标准:环境意识设计用要求 | Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design (IEC 60601-1-9:2007); German version EN 60601-1-9:2008 |
| DIN EN 60601-2-10-2003 | 医疗电气设备.第2-10部分:神经和肌肉刺激器安全性特殊要求 | Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulators (IEC 60601-2-10:1987 + A1:2001-09 + Corrigendum 1:2002); German version EN 60601-2-10:2000 + A1:2001 |
| DIN EN 60601-2-11-2005 | 医疗电气设备.第2-11部分:γ射线治疗设备安全的特殊要求 | Medical electrical equipment - Part 2-11: Particular requirements for the safety of gamma beam therapy equipment (IEC 60601-2-11:1997 + A1:2004); German version EN 60601-2-11:1997 + A1:2004 |
| DIN EN 60601-2-16-1999 | 医疗电气设备.第2-16部分:血液透析器,血液过滤器和血液过滤设备安全性的特殊要求 | Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment (IEC 60601-2-16:1998); German version EN 60601-2-16:1998 |
| DIN EN 60601-2-18-2001 | 医疗电气设备.第2-18部分:内窥设备安全性特殊要求 | Medical electrical equipment - Part 2-18: Particular requirements for the safety of endoscopic equipment (IEC 60601-2-18:1996 + A1:2000); German version EN 60601-2-18:1996 + A1:2000 |
| DIN EN 60601-2-19-2010 | 医疗电气设备.第2-19部分:婴儿保育箱的基本安全及基本性能用详细要求(IEC 60601-2-19-2009).德文版本EN 606 | Medical electrical equipment - Part 2-19: Particular requirements for basic safety and essential performance of infant incubators (IEC 60601-2-19:2009); German version EN 60601-2-19:2009 |
| DIN EN 60601-2-2-2010 | 医疗电气设备.第2-2部分:高频手术器械和高频手术器械配件的基本安全及基本性能的详细要求(IEC 60601-2-2-20 | Medical electrical equipment - Part 2-2: Particular requirements for basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories (IEC 60601-2-2:2009); German version EN 60601-2-2:2009 |
| DIN EN 60601-2-21-2010 | 医疗电气设备.第2-21部分:婴儿辐射保温箱基本安全及基本性能的详细要求(IEC 60601-2-21-2009).德文版本EN 6 | Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers (IEC 60601-2-21:2009); German version EN 60601-2-21:2009 |
| DIN EN 60601-2-22-1996 | 医疗电器设备.第2部分:诊断和治疗用激光设备安全性特殊要求 | Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 60601-2-22:1995); German version EN 60601-2-22:1996 |
| DIN EN 60601-2-23-2000 | 医疗电气设备.第2-23部分:经皮分压监护设备包括基本性能在内的安全性的特殊要求 | Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment (IEC 60601-2-23:1999); German version EN 60601-2-23:2000 |
| DIN EN 60601-2-24-1999 | 医疗电气设备.第2-24部分:注射泵和控制器安全性的特殊要求 | Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllers (IEC 60601-2-24:1998); German version EN 60601-2-24:1998 |
| DIN EN 60601-2-25-2001 | 医疗电气设备.第2-25部分:心电图安全性特殊要求 | Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs (IEC 60601-2-25:1993 + A1:1999); German version EN 60601-2-25:1995 + A1:1999 |
| DIN EN 60601-2-26-2004 | 医疗电气设备.第2-26部分:脑电图机安全的特殊要求 | Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographs (IEC 60601-2-26:2002); German version EN 60601-2-26:2003 |
| DIN EN 60601-2-29-2009 | 医疗电气设备.第2-29部分:放射线疗法模拟器的一般安全和中药性能用特殊要求 | Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators (IEC 60601-2-29:2008); German version EN 60601-2-29:2008 |
| DIN EN 60601-2-3-1999 | 医疗电气设备.第2-3部分:短波治疗设备安全性特殊要求 | Medical electrical equipment - Part 2-3: Particular requirements for the safety of short-wave therapy equipment (IEC 60601-2-3:1991 + A1:1998); German version EN 60601-2-3:1993 + A1:1998 |
| DIN EN 60601-2-30-2000 | 医疗电气设备.第2-30部分:自动循间接血压监护设备安全性的特殊要求(包括基本性能) | Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment (IEC 60601-2-30:1999); German version EN 60601-2-30:2000 |
| DIN EN 60601-2-31-2009 | 医疗电气设备.第2-31部分:用内供电源的体外心脏起博器基本安全和基本性能的特殊要求 | Medical electrical equipment - Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source (IEC 60601-2-31:2008); German version EN 60601-2-31:2008 |
| DIN EN 60601-2-33 Berichtigung 1-2009 | 医疗电气设备.第2-33部分:医疗诊断用磁共振设备安全的特殊要求.技术勘误DIN EN 60601-2-33(VDE 0750-2-33)- | Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2002 + A1:2005 + A2:2007); German version EN 60601-2-33:2002 + A1:2005 + A2:2008, Corrigendum to DIN EN 60601-2-33 (VDE 0750-2-33):2008-07; German version CENELEC-Cor.: 2008 to EN 60601-2-33:2002/A2:2008 |
| DIN EN 60601-2-33-2008 | 医用电气设备.第2-33部分:医疗诊断用磁共振设备的安全用特殊要求 | Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2002 + A1:2005 + A2:2007); German version EN 60601-2-33:2002 + A1:2005 + A2:2008 |
| DIN EN 60601-2-34-2001 | 医疗电气设备.第2-34部分:侵入式血压监测仪器安全性(包括基本性能)的特殊要求 | Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment (IEC 60601-2-34:2000); German version EN 60601-2-34:2000 |
| DIN EN 60601-2-36-1997 | 医疗电气设备.第2部分:体外碎石机安全性特殊要求 | Medical electrical equipment - Part 2: Particular requirements for the safety of equipment for extracorporeally induced lithotripsy (IEC 60601-2-36:1997); German version EN 60601-2-36:1997 |
| DIN EN 60601-2-38-2001 | 医疗电气设备.第2-38部分:电动病床安全的特殊要求 | Medical electrical equipment - Part 2-38: Particular requirements for the safety of electrically operated hospital beds (IEC 60601-2-38:1996 + A1:1999); German version EN 60601-2-38:1996 + A1:2000 |
| DIN EN 60601-2-39-2008 | 医疗电气设备.第2-39部分:腹膜透析设备基本安全和重要性能的特殊要求 | Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment (IEC 60601-2-39:2007); German version EN 60601-2-39:2008 |
| DIN EN 60601-2-40-1998 | 医疗电气设备.第2-40部分:肌电图仪和激发响应设备的安全性特殊要求 | Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromygraphs and evoked response equipment (IEC 60601-2-40:1998); German version EN 60601-2-40:1998 |
| DIN EN 60601-2-41-2010 | 医疗电气设备.第2-41部分:外科照明设备和诊断照明设备的基本安全和基本性能的特定要求 | Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis (IEC 60601-2-41:2009); German version EN 60601-2-41:2009 |
| DIN EN 60601-2-46-1999 | 医疗电气设备.第2-46部分:手术台安全性的特殊要求 | Medical electrical equipment - Part 2-46: Particular requirements for the safety of operating tables (IEC 60601-2-46:1998); German version EN 60601-2-46:1998 |
| DIN EN 60601-2-49-2002 | 医疗电气设备.第2-49部分:多功能病人监测设备安全的特殊要求 (IEC 60601-2-49:2001); 德文版本 EN 60601-2- | Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment (IEC 60601-2-49:2001); German version EN 60601-2-49:2001 |
| DIN EN 60601-2-8-2002 | 医疗电气设备.第2部分:使用范围为10kV至1MV的X射线治疗设备安全的特殊要求 (IEC 60601-2-8:1987); 德文版本 | Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the range 10 kV to 1 MV (IEC 60601-2-8:1987); German version EN 60601-2-8:1997 + A1:1997 |
| DIN EN 60613-1992 | 医疗诊断用旋转阳极X射线管的电、热和负载特性 | Electrical, thermal and loading characteristics of rotating anode X-ray tubes for medical diagnosis (IEC 60613:1989); german version EN 60613:1990 |
| DIN EN 60806-2006 | 医疗诊断用旋转阳极X-射线管最大对称辐射场的测定 | Determination of the maximum symmetrical radiation field from a rotating anode X-ray tube for medical diagnosis (IEC 60806:1984); German version EN 60806:2004 |
| DIN EN 61010-2-040-2006 | 测量、控制和实验室用电气设备的安全要求.第2-040部分:处理医疗材料用灭菌器和清洗消毒器的特殊要求(IEC 61 | Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-040: Particular requirements for sterilizers and washer-disinfectors used to treat medical materials (IEC 61010-2-040:2005); German version EN 61010-2-040:2005 |
| DIN EN 61010-2-101-2003 | 测量、控制和实验室用电气设备的安全要求.第2-101部分:体外诊断(IVD)医疗设备的特殊要求 | Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment (IEC 61010-2-101:2002, modified); German version EN 61010-2-101:2002 |
| DIN EN 61157 Berichtigung 1-2009 | 医疗诊断超声波设备声输出的报告用标准方法.技术勘误DIN EN 61157-2008-07 | Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment (IEC 61157:2007); German version EN 61157:2007, Corrigendum to DIN EN 61157:2008-07 |
| DIN EN 61157-2008 | 医疗诊断超声波设备的声输出报告用标准方法 | Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment (IEC 61157:2007); German version EN 61157:2007 |
| DIN EN 61223-2-4-2003 | 医疗成像部门的评价及例行试验.第2-4部分:稳定性试验.硬拷贝照相机 | Evaluation and routine testing in medical imaging departments - Part 2-4: Constancy tests; Hard copy cameras (IEC 61223-2-4:1994); German version EN 61223-2-4:1994 |
| DIN EN 61223-2-6-2008 | 医疗成像部门的评估和常规检验.第2-6部分:稳定性试验.计算机断层摄影X射线设备的成像性能.德文版本EN 61223 | Evaluation and routine testing in medical imaging departments - Part 2-6: Constancy tests - Imaging performance of computed tomography X-ray equipment (IEC 61223-2-6:2006); German version EN 61223-2-6:2007 |
| DIN EN 61223-3-4-2001 | 医疗放射科评定和常规试验.第3-4部分:验收试验.牙科X射线设备的成像性能 | Evaluation and routine testing in medical imaging departments - Part 3-4: Acceptance tests; Imaging performance of dental X-ray equipment (IEC 61223-3-4:2000); German version EN 61223-3-4:2000 |
| DIN EN 61223-3-5-2005 | 医疗成像部门的评价和常规检验.第3-5部分:验收试验.计算机断层摄影X射线设备的成像性能 | Evaluation and routine testing in medical imaging departments - Part 3-5: Acceptance tests - Imaging performance of computed tomography X-ray equipment (IEC 61223-3-5:2004); German version EN 61223-3-5:2004 |
| DIN EN 61262-1-1995 | 医疗电气设备.光电X射线图象增强器特性.第1部分:入口尺寸测定 | Medical electrical equipment - Characteristics of electro-optical X-ray image intensifiers - Part 1: Determination of the entrance field size (IEC 61262-1:1994); German version EN 61262-1:1994 |
| DIN EN 61262-2-1995 | 医疗电气设备.光电X射线图象增强器特性.第2部分:转换因子测定 | Medical electrical equipment - Characteristics of electro-optical X-ray image intensifiers - Part 2: Determination of the conversion factor (IEC 61262-2:1994); German version EN 61262-2:1994 |
| DIN EN 61262-3-1995 | 医疗电气设备.光电X射线图象增强器特性.第3部分:亮度分布和不均匀性测定 | Medical electrical equipment - Characteristics of electro-optical X-ray image intensifiers - Part 3: Determination of the luminance distribution and luminance non-uniformity (IEC 61262-3:1994); German version EN 61262-3:1994 |
| DIN EN 61262-4-1995 | 医疗电气设备.光电X射线图象增强器特性.第4部分:图象失真测定 | Medical electrical equipment - Characteristics of electro-optical X-ray image intensifiers - Part 4: Determination of the image distortion (IEC 61262-4:1994); German version EN 61262-4:1994 |
| DIN EN 61262-5-1995 | 医疗电气设备.光电X射线图象增强器特性.次量子系数测定 | Medical electrical equipment - Characteristics of electro-optical X-ray image intensifiers - Part 5: Determination of the detective quantum efficiency (IEC 61262-5:1994); German version EN 61262-5:1994 |
| DIN EN 61262-6-1995 | 医疗电气设备.光电X射线图象增强器特性.第6部分:对比度和伪影系数测定 | Medical electrical equipment - Characteristics of electro-optical X-ray image intensifiers - Part 6: Determination of the contrast ratio and veiling glare index (IEC 61262-6:1994); German version EN 61262-6:1994 |
| DIN EN 61262-7-2002 | 医疗电气设备.电光X射线图像增强器的特性.第7部分:调制转换功能的测定 | Medical electrical equipment - Characteristics of electro-optical X-ray image intensifiers - Part 7: Determination of the modulation transfer function (IEC 61262-7:1995); German version EN 61262-7:1995 |
| DIN EN 61267-2009 | 医疗X射线诊断设备.特性测定的放射条件 | Medical diagnostic X-ray equipment - Radiation conditions for use in the determination of characteristics (IEC 61267:2005); German version EN 612167:2006 |
| DIN EN 61303-1996 | 医疗电气设备.放射性核素准直器.性能专用规定方法 | Medical electrical equipment - Radionuclide calibrators - Particular methods for describing performance (IEC 61303:1994); German version EN 61303:1995 |
| DIN EN 61326-2-6 Berichtigung 1-2008 | 测量、控制和实验室用电气设备.电磁兼容性(EMC)的要求.第2-6部分:特殊要求.体外诊断(IVD)医疗设备.技术勘误 | Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2005); German version EN 61326-2-6:2006, Corrigendum to DIN EN 61326-2-6 (VDE 0843-20-2-6):2006-10 |
| DIN EN 61326-2-6-2006 | 测量、控制和实验室用电气设备.电磁兼容性(EMC)的要求.第2-6部分:特殊要求.实验室诊断(IVD)医疗设备(IEC 61 | Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2005); German version EN 61326-2-6:2006 |
| DIN EN 61331-2-2006 | 诊断医疗X射线的防护设备.第2部分:防护玻璃板(IEC 61331-2-1994) | Protective devices against diagnostic medical X-radiation - Part 2: Protective glass plates (IEC 61331-2:1994); German version EN 61331-2:2002 |
| DIN EN 61331-3-2002 | 医疗诊断X射线防护装置.第3部分:性腺防护服装和防护装置 (IEC 61331-3:1998); 德文版本 EN 61331-3:1999 | Protective devices against diagnostic medical X-radiation - Part 3: Protective clothing and protective devices for gonads (IEC 61331-3:1998); German version EN 61331-3:1999 |
| DIN EN 61558-2-15-2001 | 电力变压器、供电装置和类似件设备的安全性.第2-15部分:医疗场地供电用绝缘变压器的特殊要求 (IEC 61558-2- | Safety of power transformers, power supply units and similar - Part 2-15: Particular requirements for isolating transformers for the supply of medical locations (IEC 61558-2-15:1999, modified); German version EN 61558-2-15:2001 |
| DIN EN 62127-1 Berichtigung 1-2009 | 超音波学.水听器.第1部分:医疗超声波场小于40MHz的测量和特性.技术勘误DIN EN 62127-1-2008 | Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz (IEC 62127-1:2007); German version EN 62127-1:2007, Corrigendum to DIN EN 62127-1:2008-06 |
| DIN EN 62127-1-2008 | 超音波学.水听器.第1部分:医疗超声波场小于40MHz的测量和特性 | Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz (IEC 62127-1:2007); German version EN 62127-1:2007 |
| DIN EN 62127-3-2008 | 超音波学.水听器.第3部分:医疗超声波场小于40MHz的水听器的特性 | Ultrasonics - Hydrophones - Part 3: Properties of hydrophones for ultrasonic fields up to 40 MHz (IEC 62127-3:2007); German version EN 62127-3:2007 |
| DIN EN 62220-1-2-2009 | 医疗电气设备.数字X射线成像装置特性.第1-2部分:探测量子效率的测定.用于X射线照相法的探测器 | Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-2: Determination of the detective quantum efficiency - Detectors used in mammography (IEC 62220-1-2:2007); German version EN 62220-1-2:2007 |
| DIN EN 62220-1-2005 | 医疗电气设备.数字X射线制图设备的特性.第1部分:等效量子效率的测定 | Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1: Determination of the detective quantum efficiency (IEC 62220-1:2003); German version EN 62220-1:2004 |
| DIN EN 62304 Berichtigung 1-2009 | 医疗装置软件.软件寿命周期过程.技术勘误DIN EN 62304(VDE 0750-101)-2007-03 | Medical device software - Software life-cycle processes (IEC 62304:2006); German version EN 62304:2006, Corrigendum to DIN EN 62304 (VDE 0750-101):2007-03; German version CENELEC-Cor.: 2008 to EN 62304:2006 |
| DIN EN 62304-2007 | 医疗器械用软件.软件寿命过程 | Medical device software - Software life-cycle processes (IEC 62304:2006); German version EN 62304:2006 |
| DIN EN 62353-2008 | 医疗电气设备.医疗电气设备的循环试验和维修后试验 | Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment (IEC 62353:2007); German version EN 62353:2008 |
| DIN EN 62366-2008 | 医疗设备.医疗设备可用性工程的应用 | Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008 |
| DIN EN 62494-1-2010 | 医疗电气设备.数字X射线成像系统的曝光指数.第1部分:通用X射线照相术的定义和要求 (IEC 62494-1-2008); 德 | Medical electrical equipment - Exposure index of digital X-ray imaging systems - Part 1: Definitions and requirements for general radiography (IEC 62494-1:2008); German version EN 62494-1:2008 |
| DIN EN 80601-2-58-2009 | 医疗电气设备.第2-58部分:眼外科用透镜拆卸装置和玻璃体切除装置基本安全和基本性能的特殊要求(IEC 80601-2 | Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery (IEC 80601-2-58:2008); German version EN 80601-2-58:2009 |
| DIN EN 868-2-2009 | 灭菌医疗装置的包装.第2部分:灭菌套要求和测试方法,DIN EN 868-2:2009-09的英文版本 | Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods; English version of DIN EN 868-2:2009-09 |
| DIN EN 868-3-2009 | 灭菌医疗装置的包装.第3部分:生产纸袋(EN 868-4规定)和生产盒和卷筒用纸(EN 868-5规定)要求和试验方法.要求 | Packaging for terminally sterilized medical devices - Part 3: Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5) - Requirements and test methods; English version of DIN EN 868-3:2009-09 |
| DIN EN 868-4-2009 | 灭菌医疗装置的包装.第4部分:纸袋要求和测试方法,英文版本DIN EN 868-4:2009-09 | Packaging for terminally sterilized medical devices - Part 4: Paper bags - Requirements and test methods; English version of DIN EN 868-4:2009-09 |
| DIN EN 868-5-2009 | 灭菌医疗装置的包装.第5部分:多孔材料和塑料膜结构的可密封袋和卷轴.要求和测试方法,英文版本DIN EN 868-5: | Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods;English version of DIN EN 868-5:2009-09 |
| DIN EN 868-6-2009 | 灭菌医疗装置的包装.第6部分:低温灭菌处理用纸.要求和测试方法,DIN EN 868-6:2009-09的英文版本 | Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods; English version of DIN EN 868-6:2009-09 |
| DIN EN 868-7-2009 | 灭菌医疗装置的包装.第7部分:低温消毒处理用粘合铜版纸.要求和测试方法,DIN EN 868-7:2009-09的英文版本 | Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods; English version of DIN EN 868-7:2009-09 |
| DIN EN 868-9-2009 | 灭菌医疗装置的包装.第9部分:聚烯烃非包覆非织物材料.要求和测试方法,DIN EN 868-9:2009-09的英文版本 | Packaging for terminally sterilized medical devices - Part 9: Uncoated nonwoven materials of polyolefines - Requirements and test methods; English version of DIN EN 868-9:2009-09 |
| DIN EN 980-2008 | 医疗设备标注用符号 | Symbols for use in the labelling of medical devices; English version of DIN EN 980:2008-08 |
| DIN EN ISO 10524-3-2006 | 医疗气体用压力调节器.第3部分:带气缸阀的压力调节器(ISO 10524-3:2005) | Pressure regulators for use with medical gases - Part 3: Pressure regulators integrated with cylinder valves (ISO 10524-3:2005); English version of DIN EN ISO 10524-3:2006-07 |
| DIN EN ISO 10524-4-2008 | 医疗气体用压力调节器.第4部分:低压调节器 | Pressure regulators for use with medical gases - Part 4: Low-pressure regulators (ISO 10524-4:2008); German version EN ISO 10524-4:2008 |
| DIN EN ISO 10993-1-2010 | 医疗器械的生物学评价.第1部分:在风险管理系统内的评价与试验 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009); German version EN ISO 10993-1:2009 |
| DIN EN ISO 10993-11-2009 | 医疗装置生物学评定.第11部分:系统毒性试验(ISO 10993-11-2006);德文版本EN ISO 10993-11-2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006); English version of DIN ENISO 10993-11:2009-08 |
| DIN EN ISO 10993-12-2009 | 医疗器械的生物学评定.第12部分:样品制备和基准物质(ISO 10993-12:2007);德文版本EN ISO 10993-12-2009 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007); English version of DIN EN ISO 10993-12:2009-08 |
| DIN EN ISO 10993-13-2009 | 医疗装置的生物学评定.第13部分:聚合物医疗设备产生的降解物的识别和量化(ISO 10993-13-1998);德文版本EN I | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998); English version of DIN ENISO 10993-13:2009-08 |
| DIN EN ISO 10993-14-2009 | 医疗器械的生物学评定.第14部分:陶瓷降解产品的识别与量化(ISO 10993-14-2001); 德文版本EN ISO 10993-14-2 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001);English version of DIN EN 10993-14:2009-08 |
| DIN EN ISO 10993-15-2009 | 医疗设备的生物评估.第15部分:金属与合金降解产物的识别与定性(ISO 10993-15:2000,DIN EN ISO 10993-15:200 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); English version of DIN EN ISO 10993-15:2009-10 |
| DIN EN ISO 10993-17-2009 | 医疗器械的生物学评定.第17部分:可浸出物质容许限值的确定(ISO 10993-17-2002);德文版本EN ISO 10993-17-20 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002); English version of DIN EN ISO 10993-17:2009-08 |
| DIN EN ISO 10993-18-2009 | 医疗装置的生物学评定.第18部分:材料的化学表征(ISO 10993-18-2005);德文版本EN ISO 10993-18-2009 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005); English version of DIN EN ISO 10993-18:2009-08 |
| DIN EN ISO 10993-2-2006 | 医疗器械的生物评定.第2部分:动物饲养照料要求(ISO 10993-2-2006) | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006); English version of DIN EN ISO 10993-2:2006-10 |
| DIN EN ISO 10993-3-2009 | 医疗器械的生物学评价.第3部分:遗传毒性、致癌性和生殖毒性的试验(ISO 10993-3-2003); 德文版本 EN ISO 109 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003); English version of DIN EN ISO 10993-3:2009-08 |
| DIN EN ISO 10993-4-2009 | 医疗设备的生物评估.第4部分:与血液相互作用试验选择(ISO 10993-4:2002,含修改件1:2006),DIN EN ISO 10993- | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006); English version of DIN EN ISO 10993-4:2009-10 |
| DIN EN ISO 10993-5-2009 | 医疗设备的生物评估.第5部分:体外细胞毒性测试(ISO 10993-5:2009),英文标准DIN EN ISO 10993-5:2009-10 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009); English version of DIN EN ISO 10993-5:2009-10 |
| DIN EN ISO 10993-6-2009 | 医疗设备的生物学评价.第6部分:植入后局部效果试验(ISO 10993-6-2007); 德文版本 EN ISO 10993-6-2009 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007); English version of DIN EN ISO 10993-6:2009-08 |
| DIN EN ISO 10993-7-2009 | 医疗装置的生物学评定 第7部分:环氧乙烷灭菌残留物 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008); English version of DIN EN ISO 10993-7:2009-02 |
| DIN EN ISO 10993-9-2010 | 医疗器械的生物学评价 第9部分:潜在降解产物的识别与量化框架 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009); German version EN ISO 10993-9:2009 |
| DIN EN ISO 11073-10101-2006 | 健康信息学.床旁检测医疗设备通信.第10101部分:术语(ISO/IEEE 11073-10101-2004) | Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature (ISO/IEEE 11073-10101:2004); English version EN ISO 11073-10101:2005 |
| DIN EN ISO 11073-10201-2006 | 健康信息学.床旁检测医疗设备通信.第10201部分:域信息模型 | Health informatics - Point-of-care medical device communication - Part 10201: Domain information model (ISO/IEEE 11073-10201:2004); English version EN ISO 11073-10201:2005 |
| DIN EN ISO 11073-20101-2006 | 健康信息学.床旁检测医疗设备通信.第20101部分:应用轮廓.基本标准(ISO/IEEE 11073-20101:2004) | Health informatics - Point-of-care medical device communication - Part 20101: Application profiles - Base standard (ISO/IEEE 11073-20101:2004); English version EN ISO 11073-20101:2005 |
| DIN EN ISO 11073-30200-2006 | 健康信息学.床旁检测医疗设备通信.第30200部分:传输轮廓.电缆连接 | Health informatics - Point-of-care medical device communication - Part 30200: Transport profile - Cable connected (ISO/IEEE 11073-30200:2004); English version EN ISO 11073-30200:2005 |
| DIN EN ISO 11073-30300-2006 | 健康信息学.床旁检测医疗设备通信.第30300部分:传输轮廓.红外无线(ISO/IEEE 11073-30300:2004) | Health informatics - Point-of-care medical device communication - Part 30300: Transport profile - Infrared wireless (ISO/IEEE 11073-30300:2004); English version EN ISO 11073-30300:2005 |
| DIN EN ISO 11135-1-2007 | 卫生保健品灭菌.环氧乙烷.第1部分:医疗设备灭菌过程的制定、确认和常规控制的要求(ISO 11135-1-2007) | Sterilization of health care products - Ethylene oxide - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007); English version of DIN EN ISO 11135-1:2007-08 |
| DIN EN ISO 11137-1-2006 | 保健产品的灭菌.辐射.第1部分:医疗装置消毒的开发、确认和程序控制的要求(ISO 11137-1:2006) | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006) English version of DIN EN ISO 11137-1:2006-07 |
| DIN EN ISO 11138-1-2006 | 医疗保健产品灭菌.生物指示物.第1部分:一般要求 | Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2006); English version of DIN EN ISO 11138-1:2006-09 |
| DIN EN ISO 11138-4-2006 | 医疗保健产品灭菌.生物指示物.第4部分:干热灭菌过程用生物指示物 | Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2006); English version of DIN EN ISO 11138-4:2006-09 |
| DIN EN ISO 11138-5 Berichtigung 1-2007 | 医疗保健产品灭菌.生物指示器.第5部分:低温蒸汽和甲醛溶液灭菌处理用生物指示器(ISO 11138-5:2006) | Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes (ISO 11138-5:2006); German version EN ISO 11138-5:2006, Corrigenda to DIN EN ISO 11138-5:2006-09 |
| DIN EN ISO 11138-5-2006 | 医疗保健产品灭菌.生物指示物.第5部分:低温蒸汽和甲醛灭菌过程用生物指示物 | Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes (ISO 11138-5:2006); German version EN ISO 11138-5:2006 |
| DIN EN ISO 11197-2009 | 医疗供应设备(ISO 11197:2004),德文版本EN ISO 11197:2009 | Medical supply units (ISO 11197:2004); German version EN ISO 11197:2009 |
| DIN EN ISO 11607-2-2006 | 最后灭菌的医疗器械的包装.第2部分:组成、密封和装配过程的确认和要求(ISO 11607-2:2006) | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006) English version of DIN EN ISO 11607-2:2006-07 |
| DIN EN ISO 11737-1-2009 | 医疗设备的消毒.微生物法.第1部分:产品上微生物群落的测定(ISO 11737-1:2006)(含勘误表AC:2009),英文版本DI | Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006) (includes Corrigendum AC:2009); English version of DIN EN ISO 11737-1:2009-09 |
| DIN EN ISO 11737-2-2010 | 医疗器械灭菌.微生物学方法.第2部分:灭菌过程的定义、有效性和维护中进行的无菌试验(ISO 11737-2-2009); 德 | Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009); German version EN ISO 11737-2:2009 |
| DIN EN ISO 14155-1-2009 | 人体适用的医疗设备的临床调查.第1部分:一般要求(ISO 14155-1:2003)EN ISO 14155-1:2009的德文版本 | Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003); English version of DIN EN ISO 14155-1:2009-11 |
| DIN EN ISO 14155-2-2009 | 用于人体的医疗器械临床研究.第2部分:临床研究方案(ISO 14155-2:2003),EN ISO 14155-2:2009的德文版本 | Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003); English version of DIN EN ISO 14155-2:2009-11 |
| DIN EN ISO 14161-2010 | 医疗保健产品的消毒.生物指示剂.选择、使用和检验结果解释指南(ISO 14161-2009); 德文版本 EN ISO 14161-20 | Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO 14161:2009); German version EN ISO 14161:2009 |
| DIN EN ISO 14937-2010 | 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发,验证及常规控制的一般要求 (ISO 14937-2009); 德文 | Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009); German version EN ISO 14937:2009 |
| DIN EN ISO 14971-2009 | 医疗设备.风险管理在医疗设备上的应用(ISO 14971:2007,修订版2007-10-01),德文版本 EN ISO 14971:2009 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01); English version of DIN EN ISO 14971:2009-10 |
| DIN EN ISO 15002-2008 | 与医疗气体管道系统的终端装置相连接的流量计量设备 | Flow-metering devices for connection to terminal units of medical gas pipeline systems (ISO 15002:2008); English version of DIN EN ISO 15002:2008-11 |
| DIN EN ISO 15193-2009 | 体外诊断医疗设备.生物源样品中数量的测量.参考测量程序的内容和表示要求(ISO 15193:2009),DIN EN ISO 1519 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009); English version of DIN EN ISO 15193:2009-10 |
| DIN EN ISO 15225-2005 | 命名.用于管理资料交流的医疗器械命名系统规范 | Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000 + Amd 1:2004)(includes Amendment A1:2004+A2:2005); English version of DIN EN ISO 15225:2000 + A1:2004 + A2:2005 |
| DIN EN ISO 17511-2003 | 体外诊断医疗设备.生物试样中的数量测量.校准器和控制材料赋予值的测量可追踪性 | In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003); German version EN ISO 17511:2003 |
| DIN EN ISO 17664-2004 | 医疗设备的消毒.由生产商提供的可再消毒医疗设备的处理过程的信息 | Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004); German version EN ISO 17664:2004 |
| DIN EN ISO 17665-1-2006 | 保健产品的灭菌.辐射.第1部分:医疗器件消毒过程的制定、确认和常规控制的要求(ISO 17665-1:2006) | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006); English version of DIN EN ISO 17665-1:2006-11 |
| DIN EN ISO 18104-2004 | 医疗信息学.护理用参考术语模式的综合 | Health Informatics - Integration of a reference terminology model for nursing (ISO 18104:2003); German version EN ISO 18104:2003, text in English |
| DIN EN ISO 18113-1-2010 | 体外诊断医疗器械.制造商提供的信息(标签).第1部分:术语、定义和一般要求 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2009 |
| DIN EN ISO 18113-2-2010 | 体外诊断医疗器械.制造商提供的信息(标签).第2部分:专业用途的体外诊断试剂 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009); German version EN ISO 18113-2:2009 |
| DIN EN ISO 18113-3-2010 | 体外诊断医疗器械.制造商提供的信息(标签).第3部分:专业用体外诊断仪器 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2009 |
| DIN EN ISO 18113-4-2010 | 体外诊断医疗器械.制造商提供的信息(标签).第4部分:自测用体外诊断剂 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009); German version EN ISO 18113-4:2009 |
| DIN EN ISO 18113-5-2010 | 体外诊断医疗器械.制造商提供的信息(标签).第5部分:自测用体外诊断仪器 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009); German version EN ISO 18113-5:2009 |
| DIN EN ISO 18153-2003 | 体外诊断医疗设备.生物试样中的数量测量.校准器和控制材料规定的酶催化剂浓度值的测量可追踪性 | In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003); German version EN ISO 18153:2003 |
| DIN EN ISO 18779-2005 | 储存氧和氧混合物的医疗设备.特殊要求 | Medical devices for conserving oxygen and oxygen mixtures - Particular requirements (ISO 18779:2005); German version EN ISO 18779:2005 |
| DIN EN ISO 18812-2003 | 医疗信息学.临床分析仪与实验室信息系统接口.配置文件的使用 | Health informatics - Clinical analyser interfaces to laboratory information systems - Use of profiles (ISO 18812:2003); German version EN ISO 18812:2003, text in English |
| DIN EN ISO 19054-2006 | 医疗设备辅助用轨道系统 | Rail systems for supporting medical equipment (ISO 19054:2005); English version of DIN EN ISO 19054:2006-09 |
| DIN EN ISO 21171-2006 | 医疗专用手套.可移动表面粉末的测定(ISO 21171-2006) | Medical gloves - Determination of removable surface powder (ISO 21171:2006) English version of DIN EN ISO 21171:2006-08 |
| DIN EN ISO 21549-1-2004 | 医疗信息学.病人健康卡数据.第1部分:通用结构 | Health informatics - Patient healthcard data - Part 1: General structure (ISO 21549-1:2004); German and English version EN ISO 21549-1:2004 |
| DIN EN ISO 21549-2-2004 | 医疗信息学.病人健康卡数据.第2部分:通用对象 | Health informatics - Patient healthcard data - Part 2: Common objects (ISO 21549-2:2004); German version EN ISO 21549-2:2004, text in English |
| DIN EN ISO 21549-3-2004 | 医疗信息学.病人健康卡数据.第3部分:受限的临床数据 | Health informatics - Patient healthcard data - Part 3: Limited clinical data (ISO 21549-3:2004); German version EN ISO 21549-3:2004, text in English |
| DIN EN ISO 21549-4-2007 | 医疗信息.病人健康卡数据.第4部分:开放临床数据 | Health informatics - Patient healthcard data - Part 4: Extended clinical data (ISO 21549-4:2006); English version EN ISO 21549-4:2006 |
| DIN EN ISO 21549-5-2008 | 健康信息学.病人医疗卡数据.第5部分:识别数据 | Health informatics - Patient healthcard data - Part 5: Identification data (ISO 21549-5:2008); English version EN ISO 21549-5:2008 |
| DIN EN ISO 21549-6-2008 | 健康信息学.病人医疗卡数据.第6部分:管理数据 | Health informatics - Patient healthcard data - Part 6: Administrative data (ISO 21549-6:2008); English version EN ISO 21549-6:2008 |
| DIN EN ISO 21647-2009 | 医疗电气设备.呼吸气监测器的基本安全和主要性能的特殊要求(ISO 21647:2004,包括勘误表 1:2005),德文版本EN | Medical electrical equipment - Particular requirements for the basic safety and essential performance of respiratory gas monitors (ISO 21647:2004, including Cor 1:2005); German version EN ISO 21647:2009 |
| DIN EN ISO 21969-2010 | 与医疗气体系统一起使用的高压柔性连接(ISO 21969-2009).德文版本EN ISO 21969-2009 | High-pressure flexible connections for use with medical gas systems (ISO 21969:2009); German version EN ISO 21969:2009 |
| DIN EN ISO 22442-1-2008 | 医疗设备用动物组织及其衍生物.第1部分:风险管理的应用 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2007); English version of DIN EN ISO 22442-1:2008-03 |
| DIN EN ISO 22442-2-2008 | 医疗设备用动物组织及其衍生物.第2部分:来源、采集和处理控制(ISO 22442-2-2007) | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2007); English version of DIN EN ISO 22442-2:2008-03 |
| DIN EN ISO 22442-3-2008 | 医疗设备用动物组织及其衍生物.第3部分:病毒和传染性海绵状脑病(TSE)试剂的消灭和/或失效的确认 | Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007); English version of DIN EN ISO 22442-3:2008-03 |
| DIN EN ISO 7396-1-2010 | 医用气体管道系统.第1部分:压缩医疗气体和真空用管道系统(ISO 7396-1-2007 + Amd 1-2010 + Amd 2-2010).德 | Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2007 + Amd 1:2010 + Amd 2:2010); German version EN ISO 7396-1:2007 + A1:2010 + A2:2010 |
| DIN EN ISO 7405-2009 | 牙科.牙科用医疗器械的生物适应性评价(ISO 7405:2008),DIN EN ISO 7405:2009-06的英文版本 | Dentistry - Evaluation of biocompatibility of medical devices used in dentistry (ISO 7405:2008); English version of DIN EN ISO 7405:2009-06 |
| DIN EN ISO 8536-1-2008 | 医疗用注射设备.第1部分:注射玻璃瓶 | Infusion equipment for medical use - Part 1: Infusion glass bottles (ISO 8536-1:2006); German and English version EN ISO 8536-1:2008 |
| DIN EN ISO 9170-2-2009 | 医疗管道系统终端设备.第2部分:麻醉气体净化系统的终端设备(ISO 9170-2:2008),DIN EN ISO 9170-2:2009-09的 | Terminal units for medical gas pipeline systems - Part 2: Terminal units for anaesthetic gas scavenging systems (ISO 9170-2:2008); English version of DIN EN ISO 9170-2:2009-09 |
| DIN EN ISO 9187-1-2008 | 医疗用注射设备.第1部分:可注射用针剂 | Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2006); German and English version EN ISO 9187-1:2008 |
| DIN EN ISO 9626-2002 | 医疗器械用不锈钢针状管材 | Stainless steel needle tubing for manufacture of medical devices (ISO 9626:1991 + AMD 1:2001) (including amendment A1:2001); German version EN ISO 9626:1995 + A1:2001 |
| DIN EN ISO 9919-2009 | 医疗电气设备.医用脉冲血氧仪基本安全和主要性能的特殊要求(ISO 9919:2005),德文版本 EN ISO 9919:2009 | Medical electrical equipment - Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use (ISO 9919:2005); German version EN ISO 9919:2009 |
| DIN ISO 9236-1-2007 | 摄影.医疗放射照相术用屏蔽/胶片系统的感光测定.第1部分:感光曲线形状、速度和平均梯度的测定 | Photography - Sensitometry of screen/film systems for medical radiography - Part 1: Determination of sensitometric curve shape, speed and average gradient (ISO 9236-1:2004);English version of DIN ISO 9236:1:2007-08 |
| DIN V ENV 12443-2000 | 医疗信息学.保健信息框架(HIF) | Medical informatics - Healthcare Information Framework (HIF); English version ENV 12443:1999 |
| DIN V ENV 12537-1-1997 | 医疗信息技术.卫生领域电子数据交换信息项目注册.第1部分:注册人 | Medical informatics - Registration of information objects used for EDI in healthcare - Part 1: The register; English version ENV 12537-1:1997 |
| DIN V ENV 12537-2-1997 | 医疗信息技术.卫生领域电子数据交换信息项目注册.第2部分:卫生领域电子数据交换信息项目注册程序 | Medical informatics - Registration of information objects used for EDI in healthcare - Part 2: Procedures for the registration of information objects used for electronic data interchange (EDI) in healthcare; English version ENV 12537-2:1997 |
| DIN V ENV 12610-1997 | 医疗信息技术.药物识别 | Medical informatics - Medicinal product identification; English version ENV 12610:1997 |
| DIN V ENV 12611-1997 | 医疗信息技术.术语系统的类别结构.医学仪器 | Medical informatics - Categorial structure of systems of concepts - Medical devices; English version ENV 12611:1997 |
| DIN V ENV 12612-1997 | 医疗信息技术.卫生行业行政管理信息交换报文 | Medical informatics - Messages for the exchange of healthcare administrative information; English version ENV 12612:1997 |
| DIN V ENV 13606-4-2000 | 医疗保健信息学.电子保健记录信息.第4部分:信息交流用消息 | Health informatics - Electronic healthcare record communication - Part 4: Messages for the exchange of information; English version ENV 13606-4:2000 |
| DIN V ENV 13735-2001 | 健康信息学.病人与医疗装置的互操作性 | Health informatics - Interoperability of patient connected medical devices; English version ENV 13735:2000 |
| DIN V ENV 14237-2002 | 医疗保健系统的织物; 德文版本 ENV 14237:2002 | Textiles in the healthcare system; German version ENV 14237:2002 |
| DIN VDE 0100-710 Bb.1-2004 | 低压设备的安装.特殊设备或场地的要求.第710部分:医疗场所.使用DIN VDE 0100 710-2002的信息单 | Erection of low-voltage installations - Requirements for special installations or locations - Part 710: Medical locations - Information sheet for the use of DIN VDE 0100 710 (VDE 0100 Part 710):2002 11 |
| DIN VDE 0100-710-2002 | 低压装置的安装.专用设备或场所要求.第710部分:医疗场所 | Erection of low-voltage installations - Requirements for special installations or locations - Part 710: Medical locations |
| DIN VDE 0404-3-2005 | 检验电气装置安全性用测试和测量设备.第3部分:医疗电气设备或系统交付前周期性试验和试验用设备 | Testing and measuring equipment for testing the electrical safety of electrical devices - Part 3: Equipment for periodical tests and tests prior to commissioning medical electrical devices or systems |
| DIN VDE 0558-507-2008 | 医疗电气设备用基于蓄电池的中央安全电源系统 | Battery based central safety power supply systems for medical electrical equipment |
| DIN VDE 0750-209-1985 | 医用电器.微波医疗设备.安全性特殊要求 | Medical electrical equipment; part 2: particular requirements for the safety of microwave therapy equipment; identical with IEC 60601-2-6, edition 1984 |
| DIN VDE 0750-238-2002 | 医疗电气设备.第238部分:曲柄测力计安全性的特殊要求 | Medical electrical equipment - Part 238: Particular requirements for the safety of crank ergometers |
| DIN VDE 0753-2-1983 | 心脏手术用电气医疗设备使用规则.指南 | Rules relating to intracardiac applications of medical electrical equipment VDE Guide |
| DIN VDE 0753-4-2009 | 透析治疗中医疗产品的安全使用指南 | Guideline for the safe use of medical products in dialysis treatment - Text in German and English |
| DIN-Fachbericht 41-1995 | 保健中使用的已存在互换格式的句法检测.EWOS技术指南:医疗图像互换用轮廓 | Investigation of syntaxes for existing interchange formats to be used in healthcare - EWOS Technical Guide: Profiles for medical image interchange |
| DIN-Fachbericht 73-1998 | 医疗信息学.保健信息开发方法.CEN-报告 12587 | Medical informatics - Methodology for the development of healthcare messages - CEN-Report 12587 |
| DIN-Fachbericht CEN ISO/TR 14969-2005 | 医疗器件.质量管理系统.ISO 13485-2003应用指南 | Medical devices - Quality management systems - Guidance on the application of ISO 13485:2003 (ISO/TR 14969:2004); German version CEN ISO/TR 14969:2005 |
| DIN-Fachbericht CEN/TR 15133-2005 | 术语.医疗装置类的综合术语和代码 | Nomenclature - Collective terms and codes for groups of medical devices; German version CEN/TR 15133:2005 |
| DIN-Fachbericht CEN/TR 15592-2007 | 医疗卫生服务.质量管理系统.性能改善用医疗卫生服务中EN ISO 9004-2000的使用指南 | Health services - Quality management systems - Guide for the use of EN ISO 9004:2000 in health services for performance improvement |
| DIN-Fachbericht CEN/TR 15753-2008 | 包装.医疗产品用包装散页印刷品.视觉缺陷人员用盲文和其它版式 | Packaging - Package leaflets for medicinal products - Braille and other formats for visually impaired people; German version CEN/TR 15753:2008 |
| 编号 | 中文名称 | 英文名称 |