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EU/EC - MEDDEV 2.7/1

GUIDELINES ON MEDICAL DEVICES CLINICAL EVALUATION: A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES UNDER DIRECTIVES 93/42/EEC and 90/385/EEC

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Organization: EU/EC
Publication Date: 1 June 2016
Status: active
Page Count: 65

Document History

MEDDEV 2.7/1
June 1, 2016
GUIDELINES ON MEDICAL DEVICES CLINICAL EVALUATION: A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES UNDER DIRECTIVES 93/42/EEC and 90/385/EEC
A description is not available for this item.
December 1, 2009
GUIDELINES ON MEDICAL DEVICES CLINICAL EVALUATION: A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES
The primary purpose of this document is to provide manufacturers and notified bodies with guidance on how to conduct and document the clinical evaluation of a medical device as part of the conformity...
December 1, 2008
GUIDELINES ON MEDICAL DEVICES EVALUATION OF CLINICAL DATA - A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES - Appendix 1 : Clinical Evaluation of Coronary Stents
A description is not available for this item.
April 1, 2003
EVALUATION OF CLINICAL DATA: A GUIDE FOR MANUFACTURERS AND NOTIFIFIED BODIES
A description is not available for this item.

References

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