Documento fuente o registro público
In vitro diagnostic medical devices: guidance on legislation
What Great Britain actually requires of IVD sale and supply, under Part IV of UK MDR 2002.
Fuente
This document outlines the current controls on the sale and supply of in vitro diagnostic (IVD) medical devices in Great Britain and explains the main features of the requirements for IVDs, set out in Part IV of the UK Medical Devices Regulations 2002 (as amended) (UK MDR 2002).
Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.
Key takeaways
What Great Britain actually requires of IVD sale and supply, under Part IV of UK MDR 2002.
Review and references
Compiled from public manufacturer materials and regulatory sources. Not independently verified and not reviewed by a named clinician.
2026-10-09
2026-10-31
professional use
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