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Guidance document - Conformity assessment procedure - Conformity assessment of breast implants - MEDDEV 2.5/7 rev.1
Guidance document - Medical devices with a measuring function - MEDDEV 2.1/5
Guidance document - Essential requirements - “Use by”-date - MEDDEV 2.2/3 rev.3
Guidance document - Conformity assessment procedure - Subcontracting quality systems related - MEDDEV 2.5/3 rev.2
Guidance document - Field of application of directive “active implantable medical devices” - Treatment of computers used to program implantable pulse generators - MEDDEV 2.1/2.1
Guidance document - Essential requirements - Electromagnetic Compatibility (EMC) requirements - MEDDEV 2.2/1 rev.1
Guidance document - Conformity assessment procedure - Translation procedure - MEDDEV 2.5/5 rev.3
Guidance document - Conformity assessment procedure - Homogenous batches (verification of manufacturers' products) - MEDDEV 2.5/6 rev.1
Guidance document - Definitions of “medical devices”, “accessory” and “manufacturer” - MEDDEV 2.1/1
Guidance document - Field of application of directive “active implantable medical devices” - MEDDEV 2.1/2 rev.2
Guidance document - Interface with other directives – Medical devices/directive89/336/EEC relating to electromagnetic compatibility and directive 89/686/EEC relating to personal protective equipment - MEDDEV 2.1/4
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