HSA SS 436/2010
S 436/2010 is the official HSA identifier for “Health Products (Medical Devices) Regulations 2010”. S 436/2010 is the official identifier HSA uses for this instrument.
- Instrument
- S
- Full name
- S 436/2010
- Category
- General
- Authority source
- English
- Readable HTML
- 79 articles · 1 language version
- Published
- August 5, 2010
- Effective
- August 10, 2010
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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Health Products (Medical Devices) Regulations 2010
Core medical-device subsidiary legislation made under sections 45, 71 and 72 of the Health Products Act, ingested as the official informal consolidation in force from 18 December 2023 (latest amendment S 809/2023). All 79 regulation blocks across Parts I–X are in the corpus — licensing (regs 2A–2B), licence exceptions (Part II), supply and wholesaling (Part III), emergency-use exception (Part IIIA), labelling and advertisements (Parts IV–V), registration and evaluation (Part VI, including the reg 26 evaluation processes and reg 26A cancellation-for-non-payment rule), export certification (Part VII), and duties of licensees/registrants (Part VIII) — with regulation 2 definitions split per term and the Third Schedule risk-classification criteria reproduced. Numbering gaps (no reg 50; the deleted stubs 27–29 and deleted Parts/Schedules) mirror the official consolidation.
S 436/2010 is the official identifier HSA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.