| 1. |
. |
ASTM F 2451 |
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2005-APR-01 现用
Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage
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| 2. |
. |
ETSI TR 102 316 |
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2004-MAR-01 现用
Electromagnetic compatibility and Radio spectrum Matters (ERM); Ultra Low Power Animal Implantable Devices (ULP-AID) operating in the frequency band 315 kHz to 600 kHz; System Reference Document-V1.1.1
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| 3. |
. |
ASTM F 602 |
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|
2009-AUG-01 现用
Standard Criteria for Implantable Thermoset Epoxy Plastics
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| 4. |
. |
ASTM F 2129 |
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|
2008-OCT-01 现用
Standard Test Method for Conducting Cyclic Potentiodynamic Polarization Measurements to Determine the Corrosion Susceptibility of Small Implant Devices
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| 5. |
. |
CSA C22.2 NO 125-M1984 |
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1984-AUG-01 已撤销
Electromedical Equipment-General Instruction No 1-2
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| 6. |
. |
DS DSF/FprEN 60601-2-24 |
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Date NA 待定/草稿
Medical electrical equipment - Part 2-24: Particular requirements for basic safety and essential performance of infusion pumps and controllers
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| 7. |
. |
AAMI 14708-3 |
|
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2008-JAN-01 现用
Implants for surgery—Active implantable medical devices—Part 3: Implantable neurostimulators
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| 8. |
. |
AAMI 14708-4 |
|
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2008-JAN-01 现用
Implants for surgery—Active implantable medical devices—Part 4: Implantable infusion pumps
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| 9. |
. |
AAMI PC69 ERTA |
|
|
2008-JAN-01 现用
Active implantable medical devices – Electromagnetic compatibility – EMC test protocols for implantable cardiac pacemakers and implantable cardioverter
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| 10. |
. |
AFNOR NF EN 45502-1 |
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|
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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