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Class I devices

Regulatory requirements for Class I medical devices.

Official catalogue · non-binding

Class I devices guidance (1)

Catalogue entries are ordered as they appear in the European Commission catalogue.

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MDCG 2019-15 rev.1Guidance notes for manufacturers of class I medical devicesDecember 2019
Non-binding guidanceOpen guidance page
Catalogue section
Class I Devices
Published
December 2019
Topics

Source document

  • MDCG 2019-15 rev.1PDF · Unverified extraction previewOfficial source

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