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NMPB RMd

RMd/R/01/01, Issue 3 (1 August 2019)

Requirements for the registration of Medical Devices (Human and Veterinary)
SudanNational Medicines and Poisons Board / Federal Ministry of HealthRegistrationExpired
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Expired. This text is retained for historical reference.

What this code is

RMd/R/01/01, Issue 3 (1 August 2019) is the official NMPB identifier for “Requirements for the registration of Medical Devices (Human and Veterinary)”. RMd/R/01/01, Issue 3 (1 August 2019) is the official identifier NMPB uses for this instrument.

Instrument
RMd
Full name
RMd/R/01/01, Issue 3 (1 August 2019)
Category
Registration
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About this regulation

Requirements for the registration of Medical Devices (Human and Veterinary)

Complete single-page NMPB registration requirements covering manufacturing-site registration, application, fees, acceptable certificates, device description/intended use and labelling for human and veterinary devices. The original footer identifies issue 3 dated 1 August 2019 and an expiry date of 1 August 2022. It remains available on the authority website, but is retained as a dated source and must not be treated as a verified current checklist.

RMd/R/01/01, Issue 3 (1 August 2019) is the official identifier NMPB uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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