SAHPRA SAHPGL-MD-22SAHPGL-MD-22 Version 1
Medical Device Regulatory Reliance Guideline
South AfricaSouth African Health Products Regulatory AuthorityRegistrationEffective February 25, 2026
What this code is
SAHPGL-MD-22 Version 1 is the official SAHPRA identifier for “Medical Device Regulatory Reliance Guideline”. SAHPGL-MD-22 Version 1 is the official identifier SAHPRA uses for this instrument.
- Instrument
- SAHPGL-MD-22
- Full name
- SAHPGL-MD-22 Version 1
- Category
- Registration
Source links
- Authority source
- English
- Readable HTML
- Not available yet
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Use the official source while a readable HTML version is being prepared.
Dates
- Published
- —
- Effective
- February 25, 2026
About this regulation
Medical Device Regulatory Reliance Guideline
Defines reliance pathways SAHPRA may use for device and IVD registration, establishment licensing, clinical trials, ISO 13485 audits, and post-market activities.
SAHPGL-MD-22 Version 1 is the official identifier SAHPRA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.