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How to comply with the MDR requirements for medical device labels | #iso 13485 Certification in South Africa # ISO 13485 Certification in Philippines # ISO 13485 Certification in qatar # ISO 13485 Certification in chennai # ISO 13485 Certification in Iraq

How to comply with the MDR requirements for medical device labels

How to comply with the MDR requirements for medical device labels

According to the definitions in the European Union’s Medical Device Regulation (MDR) “label” ability any written, printed, or image statistics acting both on the system itself, or on the packaging of every unit or on the packaging of a couple of devices.