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Medical Devices: Post Market Surveillance: National Competent Authority Report Exchange Criteria and Report Form : SG2(PD)/N79R5 Study Group 2 – Proposed Document
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Document Date: 2012-11-13 17:52:52

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File Size: 98,50 KB

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Company

Class I / SG2 / Authoring Group / /

Country

Canada / /

Event

Product Recall / Product Issues / /

IndustryTerm

subject device / implantable devices / device / clinical management / diagnostic device / Software version / software upgrades / voluntary / /

Organization

FDA / European Union / NCAR Secretariat / Global Harmonization Task Force / /

Position

authorized representative / representative / Reporter / authorised representative / /

Product

Manufacturer Ref/ / notifications / /

SocialTag