MIR Form 7.3.1 is now mandatory in Europe and Switzerland, replacing the old version (MIR 7.2.1). For more information, please […]
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2 events,Manufacturers with IVDD legacy devices up-classed to Class C under the IVDR, must have lodged an application with a Notified […] Class III implantable custom-made devices (CMDs) must comply with the MDR in order to continue being placed on the market, […] |
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1 event,Use of the EUDAMED 1) Actor, 2) UDI/Device, 3) Notified Bodies/Certificates, and 4) Market Surveillance modules come into force today. […] |
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