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CE marking of general medical devices 11 CE marking of general medical devices that come within the scope of more than one Directive 12 Exemptions from regulations 8 and 10 13 Procedures for affixing a CE marking to general medical devices 14 Procedures for systems and procedure packs and for devices to be sterilised before use 15 Procedures for custommade.
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Unique Device Identification Direct Marking of Devices Guidance for Industry and Food and Drug Administration Staff Figure 2 1 Implantable devices are not subject to.
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CE Marking Manufacturer Commercial Name ID Method Target Format Navigate Yes CE Marking Yes A&B The database contains publicly available In Vitro Diagnostic Medical Devices for COVID19 and it is being updated periodically Please note that additional performance (as retrieved from manufacturers web pages) is provided only for devices commercially available.
