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EEC 2012/722/EC

Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin

Directive by European Union Directives , 08/08/2012

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Full Description

EEC 2012/722/EC lays down particular requirements in relation to the placing on the market and/or putting into service of medical devices, including active implantable medical devices, manufactured utilising animal tissue which is rendered non-viable or non-viable products derived from animal tissue.
 

Product Details

Published:
08/08/2012
Number of Pages:
10
File Size:
1 file , 760 KB
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This product is unavailable in Russia, Ukraine, Belarus
 

Document History

  1. EEC 2012/722/EC

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    Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin

    • Most Recent

  2. EEC 2003/32/EC


    Commission Directive 2003/32/EC introducing detailed specifications as regards the requirements laid down in Council Directive 93/42/EEC with respect to medical devices manufactured utilising tissues of animal origin

    • Historical Version