AIMDD Horizontal Harmonized Standards
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EN ISO 10993-1

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process more

EN ISO 10993-04

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood more

EN ISO 10993-05

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity more

EN ISO 10993-06

Biological evaluation of medical devices - Part 6: Tests for local effects after implantation more

EN ISO 10993-07

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals more

EN ISO 10993-09

Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products more

EN ISO 10993-11

Biological evaluation of medical devices - Part 11: Tests for systemic toxicity more

EN ISO 10993-12

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials more

EN ISO 10993-13

Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices more

EN ISO 10993-16

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables more

EN ISO 10993-17

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances more

EN ISO 10993-18

Biological evaluation of medical devices - Part 18: Chemical characterization of materials more

EN ISO 14155

Clinical investigation of medical devices for human subjects - Good clinical practice more

EN 45502-1

Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer more

EN 45502-2-1

Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers) more

EN 45502-2-2

Active implantable medical devices -- Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators) more

EN 45502-2-3

Active implantable medical devices -- Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems more

EN 62304

Medical device software - Software life-cycle processes more

EN 60601-1

Medical electrical equipment -- Part 1: General requirements for basic safety and essential performance more

EN 60601-1-6

Medical electrical equipment -- Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability more

EN 1041

Information supplied by the manufacturer of medical devices more

EN ISO 13408-1

Aseptic processing of health care products - Part 1: General requirements more

EN ISO 13408-2

Aseptic processing of health care products - Part 2: Filtration more

EN ISO 13408-3

Aseptic processing of health care products - Part 3: Lyophilization more

EN ISO 13408-6

Aseptic processing of health care products - Part 6: Isolator systems more

EN ISO 13485

Medical devices - Quality management systems - Requirements for regulatory purposes more

EN ISO 14971

Medical devices - Application of risk management to medical devices more

EN 556-1

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices more

EN 556-2

terilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices more

EN ISO 11135-1

Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices more

EN ISO 11137-1

Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices more

EN ISO 11137-2

Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose more

EN ISO 11138-3

Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes more

EN ISO 11138-2

Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes more

EN ISO 11140-1

Sterilization of health care products - Chemical indicators - Part 1: General requirements more

EN ISO 11607-1

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems more

EN ISO 11737-1

Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products more

EN ISO 11737-2

Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process more

EN ISO 14937

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 more

EN ISO 17665-1

Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices more