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¡ñ Ò½ÓõçÆ÷É豸¼ì²â³ß¶È / Medical Device testing standards list
Ãû³Æ |
¹ú¼Ê³ß¶È |
¹úÄÚ³ß¶È |
Ò½ÓõçÆøÉ豸 µÚ2²¿ÃÅ Ðĵçͼ»úÄþ¾²×¨ÓÃÒªÇó Medical safety and electrical essential equipment performance - Part 2-25: of electrocardiographs Particular requirements |
IEC/EN 60601-2-25 |
GB 10793 |
ÎÞ´´ÑªÑ¹¼ÆµÚ1²¿ÃÅ:ͨÓÃÒªÇó Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type |
EN ISO /ISO 81060-1 |
|
ÎÞ´´ÑªÑ¹¼Æ.µÚ3²¿ÃÅ:µç-»úѪѹÕÉÁ¿ÏµÍ³µÄÔö²¹ÒªÇó Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems |
EN 1060-3
|
|
Ò½ÓõçÆøÉ豸 µÚ2-27²¿ÃÅ£ºÐĵç¼à»¤Äþ¾²¼°»ùÌìÐÔÄÜרÓÃÒªÇó Medical electrical equipment - Part 2-27: Particular requirements for the basi csafety and essential performance of electrocardiographic monitoring equipment |
IEC/EN 60601-2-27
|
GB 9706.25 |
Ò½ÓõçÆøÉ豸 µÚ2-26²¿ÃÅ£ºÄÔµçͼ»úÄþ¾²×¨ÓÃÒªÇó Medical electrical equipment-Part 2-26: Particular requirements for the safety of electroencephalographs |
IEC/EN 60601-2-26:2012 |
GB 9706.26 |
Ò½ÓõçÆøÉ豸 µÚ2-56²¿ÃÅ:ÁÙ´²ÌåμƵĻù±¾Äþ¾²ºÍÐÔÄܵÄרÓÃÒªÇó Medical safety and electrical essential equipment-Part performance2-56: of clinical Particular thermometers requirements for basic body temperature measurement |
ISO/ EN ISO 80601-2-56 |
YY 9706.256 |
Ѫѹ¼Æ Non-invasive automated sphygmomanometers |
ANSI/AAMI SP10 |
YY 0670 |
Ò½ÓõçÆøÉ豸--µÚ2-57²¿ÃÅ:ÖÎÁÆ¡¢Õï¶Ï¡¢¼à²âºÍÃÀÈÝ/ÃÀѧʹÓõķǼ¤¹â¹âÔ´É豸µÄ»ù±¾Äþ¾²ºÍ»ùÌìÐÔÄÜרÓÃÒªÇó Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic,diagnostic,monitoring and cosmetic/aesthetic use |
IEC/EN 60601-2-57
|
YY 9706.257 |
Ò½ÓõçÆøÉ豸 µÚ2-2²¿ÃÅ:¸ßƵÊÖÊõÉ豸Äþ¾²×¨ÓÃÒªÇó Medical Basic Safety Electrical And Equipment Essential -Performance Part 2-2: Particular Of High Requirements Frequency For Surgical Equipment And High Frequency Surgical Accessories |
IEC/EN/EN IEC 60601-2-2 |
GB 9706.4 |
Ò½ÓõçÆøÉ豸µÚ1²¿ÃÅ£ºÄþ¾²Í¨ÓÃÒªÇó Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ANSI/AAMI ES60601-1 |
GB9706.1 |
Ò½ÓõçÆøÉ豸µÚ2-10²¿ÃÅ:Éñ¾ºÍ¼¡Èâ´Ì¼¤Æ÷Äþ¾²×¨ÓÃÒªÇó Medical electrical equipment - Part 2-10 : particular requirements for the safety of nerve and muscle stimulators |
IEC/EN 60601-2-10
|
YY 0607 |
Ò½ÓõçÆøÉ豸 µÚ2-30²¿ÃÅ:×Ô¶¯Ñ»·ÎÞ´´ÑªÑ¹¼à»¤É豸µÄÄþ¾²ºÍ»ùÌìÐÔÄÜרÓÃÒªÇó Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers |
|
YY 0667 |
Ò½ÓõçÆøÉ豸 µÚ2-49²¿ÃÅ£º¶à²ÎÊý»¼Õ߼໤É豸Äþ¾²×¨ÓÃÒªÇó Medical electrical equipment-Part 2-49:Particular requiremens for the safety of multifunction patient monitoring equipment |
IEC/EN 80601-2-49 |
YY 0668 |
Ò½ÓõçÆøÉ豸.Ò½ÓÃÂö²«ÑªÑõÒÇÉ豸»ù±¾Äþ¾²ºÍÖ÷ÒªÐÔÄÜרÓÃÒªÇó Medical electrical equipment — Part 2-61: Particular requirements for basic safetyand essential performance of pulseoximeter equipment |
ISO / EN ISO 80601-2-61
|
YY 0784 |
Ò½ÓõçÆøÉ豸 µÚ2-38²¿ÃÅ:Ò½Ôºµç¶¯´²Äþ¾²×¨ÓÃÒªÇó Medical electrical equipment - Part 2: Particular requirements for the safety of electrically operated hospital beds |
|
YY 0571 |
ÐĵçÕï¶ÏÉ豸 Diagnostic electrocardiographic devices |
ANSI/AAMI EC11 |
YY 1139 |
Ò½ÓõçÆøÉ豸 µÚ1-11²¿ÃÅ£ºÄþ¾²¼°»ùÌìÐÔÄܵÄͨÓÃÒªÇó—²¢Áг߶ȣº¼ÒÍ¥Ò½ÁƱ£½¡»·¾³ÏÂʹÓõÄÒ½ÓõçÆøÉ豸ºÍϵͳ Part 1-11: General requirements for basic safety and essential performance –Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment |
IEC/EN 60601-1-11
|
YY 9706.111 |
Ò½ÓÃÌåμÆ.×î´ó×°ÖÃСÐ͵çÌåμÆ(·ÇÔ¤²âÐͺÍÔ¤²âÐÍ)µÄÐÔÄÜ Performance of compact electrical thermometers (non-predictive and predictive) with maximum device |
EN 12470-3 |
|
ÁÙ´²ÌåμÆ.Á¬ÐøÕÉÁ¿Óõç×ÓÌåμƵÄÐÔÄÜ Performance of electrical thermometers |
EN 12470-4 |
YY 0785 |
ºìÍâÌåÎÂ¼Æ infrared ear thermometers (with maximum device)
|
EN 12470-5
|
GB/T 21417.1 |
Ò½ÓõçÆøÉ豸 µÚ2²¿ÃÅ£º¶¯Ì¬ÐĵçͼϵͳÄþ¾²ºÍ»ùÌìÐÔÄÜרÓÃÒªÇó Part 2-47: Particular requirements for the basic safety and essential performance of ambulatory electrocardiographic systems |
IEC/EN 60601-2-47 |
YY 0885 |
Ò½ÓõçÆøÉ豸 µÚ2²¿ÃÅ£ºÕï¶ÏºÍÖÎÁƼ¤¹âÉ豸Äþ¾²×¨ÓÃÒªÇó Part 2-22: Particular requirements for basic safety and essential performance of surgical,cosmetic,therapeutic and diagnostic laser equipment |
IEC/EN 60601-2-22
|
GB 9706.20 |
Ò½ÓõçÆøÉ豸.µÚ2²¿ÃÅ:ÊÖÊõÎÞÓ°µÆºÍÕï¶ÏÓÃÕÕÃ÷µÆÄþ¾²×¨ÓÃÒªÇó Part 2-41: Particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis |
IEC/EN 60601-2-41 |
YY 0627 |
Ò½ÓõçÆøÉ豸 µÚ2²¿ÃÅ£ºÊÖÊǫ̃Äþ¾²×¨ÓÃÒªÇó Part 2-46: Particular requirements for the basic safety and essential performance of operating tables |
IEC/EN 60601-2-46
|
YY 0570 |
Ðĵç¼à»¤ÒǵçÀº͵¼ÁªÏß ECG trunk cables and patient leadwires |
AAMI ANSI EC53 |
YY 0828 |
Ò½ÓõçÆøÉ豸 µÚ2-18²¿ÃÅ:ÄÚ¿ú¾µÉ豸Äþ¾²×¨ÓÃÒªÇó Part performance 2-18: Particular of endoscopic requirements equipment |
IEC/EN 60601-2-18
|
GB9706.19 |
Ò½ÓõçÆøÉ豸 µÚ1-2 ²¿ÃÅ£ºÄþ¾²Í¨ÓÃÒªÇó ²¢Áг߶ȣºµç´Å¼æÈÝ ÒªÇóºÍÊÔÑé Medical electrical equipment-Part 1-2:General requirements for safetyCollateral standard :Electromagnetic compatibility-Requirements and tests |
IEC/EN 60601-1-2
|
YY 0505 YY9706.102 |
Ò½ÓõçÆøÉ豸 - µÚ1-8 ²¿ÃÅ:»ù±¾Äþ¾²ºÍ»ùÌìÐÔÄܵÄͨÓÃÒªÇó - ²¢Áг߶È: ͨÓÃÒªÇó£¬Ò½ÁƵçÆøÉ豸ºÍÒ½ÁƵçÆøϵÖÐͳ±¨¾¯ÏµÍ³µÄ²âÊÔºÍÖ¸ÄÏ Medical electrical equipment- Part 1-8: General requirements for safety Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems |
IEC/EN 60601-1-8
|
YY0709 |
¼¤¹â²úÎïµÄÄþ¾² µÚ1 ²¿ÃÅ:É豸·ÖÀàºÍÒªÇó Safety of laser products —Part 1: Equipment classification and requirements |
IEC/EN 60825-1 |
GB 7247.1 |
µÆºÍµÆϵͳµÄ¹âÉúÎïÄþ¾²ÐÔ Photobiological safety of lamps and lamp systems |
IEC /EN62471 |
GB/T 20145 |
ºôÎüÖÎÁÆÉ豸,µÚ1²¿ÃÅ:Îí»¯ÏµÍ³¼°Æä×é³É²¿ÃÅ RESPIRATORY THERAPY EQUIPMENT –Part 1: Nebulizing systems and their components |
EN13544-1 |
YY 0109 |
Ò½ÓõçÆøÉ豸--µÚ2-24²¿ÃÅ:ÊäÒº±Ã¼°¿ØÖÆÆ÷µÄ»ù±¾Äþ¾²ºÍ»ùÌìÐÔÄÜרÓÃÒªÇó Medical electrical equipment –Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers |
IEC/EN 60601-2-24
|
GB 9706.27 |
Ò½ÓõçÆøÉ豸--µÚ2-34²¿ÃÅ:Óд´ÑªÑ¹¼à»¤É豸µÄ»ù±¾Äþ¾²ºÍ»ùÌìÐÔÄÜרÓÃÒªÇó Medical electrical equipment - Part 2-34: Particular requirementsfor the basic safety and essential performance of invasive bloodpressure monitoring equipment |
IEC/EN 60601-2-34
|
YY0783 |
Ò½ÓõçÆøÉ豸 2-60²¿ÃÅ£ºÑÀ¿ÆÉ豸µÄ»ù±¾Äþ¾²ºÍ»ùÌìÐÔÄÜ Medical electrical equipment –Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment |
IEC/EN 80601-2-60
|
GB 9706.260 |
Ò½ÓÃÉ豸 - µÚÒ»²¿ÃÅ£ºÒ½ÓÃÉ豸¿ÉÓÃÐÔ¹¤³ÌµÄÓ¦Óà Medical devices IEC devices 62366-1: - Part 2015 1: IEC Application 62366: 2007+A1:2014 of usability engineering |
IEC/EN 62366-1
|
YY/T 1474 |
Ò½ÓõçÆøÉ豸 - µÚ1-6²¿ÃÅ£º»ù±¾Äþ¾²ºÍ»ùÌìÐÔÄܵÄͨÓÃÒªÇó - ²¢Áг߶ȣº¿ÉÓÃÐÔ Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral s tandard: Usability |
IEC/EN 60601-1-6
|
YY/T 9706.106 |
Ò½ÓõçÆøÉ豸 µÚ2²¿ÃÅ:Ó¤¶ùÅàÑøÏäÄþ¾²×¨ÓÃÒªÇó Medical electrical equipment -Part 2:Particular requirements for safety of baby incubators |
IEC/EN 60601-2-19
|
GB 9706.219 |
Ò½ÁƵçÆøÉ豸-µÚ1-9²¿ÃÅ:»ù±¾Äþ¾²ºÍÖØÒªÐÔÄܵÄÒ»°ãÒªÇó.Á¥Êô³ß¶È:»·¾³ÒâʶÉè¼ÆµÄÒªÇó Medical electrical equipment Part 1-9: General requirements for basic safety and essential performance –Collateral Standard: Requirements for environmentally conscious design |
IEC/EN 60601-1-9
|
|
Ò½Óõç×ÓÌåÎÂ¼Æ Clinical electronic thermometer |
|
GB/T21416 |
Ò½ÁÆÆ÷еÈí¼þ Èí¼þÉú´æÖÜÆÚ¹ý³Ì Medical device software — Software life cycle processes |
IEC62304
|
YY/T 0664 |
Ò½ÓÃÎüÒýÉ豸 µÚ1²¿ÃÅ: µç¶¯ÎüÒýÉ豸 Äþ¾²ÒªÇó Medical suction equipment Part 1: Electrically powered suction equipment — Safety requirements |
ISO10079-1
|
YY/T 0636.1 |
Ò½ÓõçÆøÉ豸 µÚ2-37²¿ÃÅ£º³¬ÉùÒ½ÁÆÕï¶Ï¼àÊÓÉ豸»ù±¾Äþ¾²ºÍ»ùÌìÐÔÄܵÄÌØÊâÒªÇó Medical electrical equipment —Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment |
IEC/EN 60601-2-37 |
GB 9706.9 |
Ò½Óó¬ÉùÕï¶ÏÉ豸ÉùÊä³öÐû²¼ÒªÇó Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment |
IEC 61157 |
GB/T16846 |
Ò½ÁÆÕï¶Ï³¬Éù²¨É豸µÄÉùÊä³ö³ÂËßÓó߶ÈÒªÁì Ultrasonics dental descaler systems; measurement and declaration of the output characteristics |
IEC 61205 |
YY/T 0751 |
³¬Éù¶àÆÕÀÕÌ¥¶ùÐÄÂÊÒÇ ultrasonic Doppler fetal heartbeat detector |
|
YY 0448 |
³¬Éù¶àÆÕÀÕÌ¥¶ù¼à»¤ÒÇ ultrasonic Doppler fetal monitor |
|
YY/T0449 |
³¬ÉùÀíÁÆÉ豸 Medical electrical equipment —Part 2-5: Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment |
IEC/EN 60601-2-5 |
YY/T1090
|
³¬Éù Ë®ÌýÆ÷ µÚ1²¿ÃÅ£º40MHz ÒÔÏÂÒ½Óó¬Éù³¡µÄÕÉÁ¿ºÍÌØÕ÷Ãè»æ ultrasonic-Hydrophone Part 1: Measurement and characterization of medical ultrasonic fields to 40MHZ |
IEC62127-1 |
YY/T 0865.1 |
Ò½ÓÃÄÚ¿ú¾µ |
IEC/EN 60601-2-18 |
YY 0068.1 |
Ò½ÓýºÄÒʽÄÚ¿ú¾µ |
|
YY 1298 |
Ò½ÓÃÄÚ¿ú¾µÕÕÃ÷ÓùâÀ |
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YY/T 0763 |
Ò½Óõç×ÓÄÚ¿ú¾µ |
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YY 1587 |
Ò½ÓÃÄÚ¿ú¾µ ÄÚ¿ú¾µ¹¦Ð§¹©Ó¦×°Öà ÉãÏñϵͳ |
|
YY/T1603 |
»·¾³ÊÔÑéÒªÇó¼°ÊÔÑéÒªÁì |
|
GB/T14710 |
²úÎï¼ÓËÙÀÏ»¯ÊÔÑéÒªÁì |
IEC62506 |
GB/T34986 |
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