NMPB RMdRMd/R/01/03, Issue 3 (16 August 2020)
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
RMd/R/01/03, Issue 3 (16 August 2020) is the official NMPB identifier for “The registration of Medical Devices (Content of the Label)”. RMd/R/01/03, Issue 3 (16 August 2020) is the official identifier NMPB uses for this instrument.
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- RMd/R/01/03, Issue 3 (16 August 2020)
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The registration of Medical Devices (Content of the Label)
Complete two-page NMPB controlled guidance, RMd/R/01/03 issue 3, dated 16 August 2020, with printed controlled-copy expiry of 16 August 2023. Clauses a–q cover label location, trade name, identification, manufacturer/importer details, IVD indication, lot/serial/version information, expiry/manufacture date, quantities, storage, sterility, precautions, single use, custom-made devices and separate kit reagents. Both pages and all footer information were visually checked. The same-body stamped scan ce89cf6b… is retained as an alternate expression, not a second instrument. Printed copy expiry is not treated as proof of legal repeal; a renewed controlled copy and applicability in 2026 remain unverified.
RMd/R/01/03, Issue 3 (16 August 2020) is the official identifier NMPB uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.