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Medsafe SR

SR 2003/325

Medicines (Database of Medical Devices) Regulations 2003
New ZealandMinistry of Health — MedsafeRegistration
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What this code is

SR 2003/325 is the official Medsafe identifier for “Medicines (Database of Medical Devices) Regulations 2003”. SR 2003/325 is the official identifier Medsafe uses for this instrument.

Instrument
SR
Full name
SR 2003/325
Category
Registration
Source links
Authority source
English
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Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
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37 articles · 1 language version
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Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
November 17, 2003
Effective
—
Consolidated through
2020-08-07
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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.

English full text37 articles · English — reprint as at 7 August 2020Read HTML →
About this regulation

Medicines (Database of Medical Devices) Regulations 2003

Regulations establishing the statutory notification database for medical devices supplied in New Zealand (administered by Medsafe as the WAND database). Official reprint as at 7 August 2020, made under section 105 of the Medicines Act 1981: regulations 1-15 cover the database, sponsor information and declaration duties, prohibited statements, and offences, with Schedule 1 exempt devices and the Schedule 2 risk-classification rules (clauses 1-22) carried as citeable clause anchors.

SR 2003/325 is the official identifier Medsafe uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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