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When Should I Change My Basic Udi? [Solved]
In particular, a new UDI-DI shall be required in the case of any change of the following elements: name or trade name, device version or model, labelled as single use, packaged sterile, need for sterilization before use, quantity of devices provided in a package, critical warnings or contra-indications (e.g. containing
Basic UDI-DI (English Version)
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How to create your UDI with Sylvia Reingardt from GS1
In this video, we
UDI requirements for medical device manufacturers in the EU
Chapters: 00:00 Introduction 00:15 About
