The European Commission published its recommendation for a common framework (...)
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MME News
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16 June 2013
UDI, Eudamed and Medical Device Regulation
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27 April 2013
The 2013 Revision Of The EU Vigilance Guidelines
Revision 8 of MEDDEV 2.12-1, the new European Medical Device Vigilance (...)
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15 February 2013
EU Medical Device Regulation’s Scrutiny Procedure Could Hinder CE Marking Process
As soon as the European Commission published the proposed new European (...)
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27 November 2012
The new French Decree: Advertising visa for high risk medical devices
The French decree regarding the list of medical devices for which (...)
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27 September 2012
EU Medical Device Directive Revision - What’s going on ?
The publication of the Commission’s revision proposal to the Council and (...)
Last News
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27 May 2020
May 2020 - 17th Notify Body designated by NANDO
May 2020 - 17th Notify Body designated by NANDO
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7 May 2020
New ISO 9001-2015 Certificate for MediMark Europe
Company:MEDIMARK EUROPE Sarl / Site Name:MEDIMARK EUROPE SarlAddress:11 Rue Emile Zola, Grenoble, France (Metropolitan)
Certificate #:10000244364-MSC-COFRAC-FRAAccreditation:COFRAC
Standard:ISO 9001:2015
Status:Issued/Current
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17 April 2020
April 17th EU parliament voting MDR postponing
MDR 2017/745 postponed till May 2021
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31 March 2020
March 2020 - NANDO designated NBs MDR-IVDR
March 2020 Update of the list of Notified Bodies accredited by NANDOfor MDR and IVDR
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13 March 2020
2020-02- NANDO NBs Update - NSAI 0050
Designation by NANDO of NSAI as MDR NB
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