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PMS and QMS (ISO 13485) relationship in line with MDR

The Post Market Surveillance Procedure complies with MEDDEV 2.12/1, European Medical Device Regulation MDR 2017/745, (EN) ISO 13485:2016.

PMCF

INDIA – Bangalore
+ 91 994 591 2081
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USA – Chicago
+1 630 696 1293
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GERMANY – Bremen
+49 2161 990 8831
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