MDR European Medical Device Distributor Template
The European Commission in the Medical Device Regulations (MDR) has imposed many legal obligations on the European Medical Device Distributors. These legal obligations require you, a Distributor to maintain several registers which include, but are not limited to, Complaints, Device Verification, Class III implantable, and Vigilance.
Following direct industry requests Eudamed.eu, using their extensive MDR and EUDAMED experience, have prepared spreadsheet templates specifically for you the European Distributor. These templates will assist you in meeting your many Distributor legal obligations.
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