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ISAF Law

Law No. 12/2025

Medical Device Supervision and Administration Regime
MacauPharmaceutical Administration BureauGeneralEffective July 1, 2026
What this code is

Law No. 12/2025 is the official ISAF identifier for “Medical Device Supervision and Administration Regime”. Law No. 12/2025 is the official identifier ISAF uses for this instrument.

Instrument
Law
Full name
Law No. 12/2025
Category
General
Source links
Authority source
Chinese and Portuguese
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Readable HTML
Not available yet
Use the official source while a readable HTML version is being prepared.
Dates
Published
—
Effective
July 1, 2026
About this regulation

Medical Device Supervision and Administration Regime

Macau’s lifecycle framework for medical device registration or filing, clinical investigation, manufacturing, import/export, wholesale, retail, supply and post-market control. The official portal is available; a multi-instrument bilingual compilation is not treated as a single citeable expression of Law 12/2025.

Law No. 12/2025 is the official identifier ISAF uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.