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NMPB RMd

RMd/R/01/02, Issue 3 (16 August 2020)

The registration of Medical Devices (Description of product)
SudanNational Medicines and Poisons Board / Federal Ministry of HealthRegistrationExpired
Document status

Expired. This text is retained for historical reference.

What this code is

RMd/R/01/02, Issue 3 (16 August 2020) is the official NMPB identifier for “The registration of Medical Devices (Description of product)”. RMd/R/01/02, Issue 3 (16 August 2020) is the official identifier NMPB uses for this instrument.

Instrument
RMd
Full name
RMd/R/01/02, Issue 3 (16 August 2020)
Category
Registration
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Source publication
English
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About this regulation

The registration of Medical Devices (Description of product)

Complete single-page NMPB controlled document, issue 3 dated 16 August 2020, with a printed expiry date of 16 August 2023. Retained as a dated source and excluded from default current discovery; the authority’s continuing link and the filename NEW do not establish a renewed version. Lists the STED product-description elements, including intended use, patient population, operating principle, class and classification rule, novel features, accessories and combinations, all configurations/variants, key components including software, patient-contact materials and specifications. The complete native text, control footer and original page image are preserved. The issue and controlled-copy expiry dates do not themselves prove when an underlying legal obligation commenced or ceased. A verified replacement, current applicability and separate variation rules remain under review.

RMd/R/01/02, 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.