| 1. |
. |
DS ISO 14708-1 |
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Date NA 现用
Implants for surgery - Active implantable medical devices - Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
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| 2. |
. |
AAMI 80601-2-58 |
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2008-JAN-01 现用
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
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| 3. |
. |
AAMI TIR16142 |
|
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2005-JAN-01 现用
Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices-2006 printing
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| 4. |
. |
AFNOR NF EN 45502-1 |
|
|
1998-NOV-01 现用
Active implantable medical devices. Part 1 : general requirements for safety, marking and information to be provided by the manufacturer.
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| 5. |
. |
AFNOR NF EN 60601-2-45 |
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|
2005-NOV-01 现用
Medical electrical equipment - Part 2-45 : particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices
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| 6. |
. |
AFNOR NF EN 80601-2-58 |
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|
2009-APR-01 现用
Medical electrical equipment - Part 2-58 : particular requirements for basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery
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| 7. |
. |
AFNOR NF EN ISO 10651-6 |
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|
2004-DEC-01 现用
Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6 : home care ventilatory support devices
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| 8. |
. |
AFNOR NF EN ISO 10651-6 |
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|
2009-JUL-01 现用
Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6 : home-care ventilatory support devices
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| 9. |
. |
ASTM F 2503 |
|
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2008-OCT-01 现用
Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment
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| 10. |
. |
BSI BS EN 45502-1 |
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|
1998-FEB-15 现用
Active Implantable Medical Devices Part 1: General Requirements for Safety, Marking and Information to be Provided by the Manufacturer
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