2 docs tagged with "ukrp"

Which entities are required to register with MHRA before placing medical devices on the Great Britain market — manufacturers, UK Responsible Persons, and authorised representatives — and the consequences of failing to register.

The economic operators with obligations under the UK Medical Devices Regulations 2002 — manufacturers, UK Responsible Persons (UKRPs), importers, distributors, and authorised representatives — and what each role requires.