MCAZ SRSR 03 Rev 7
SR 03 Rev 7 is the official MCAZ identifier for “Sample Receipt Form - Medical Devices”. SR 03 Rev 7 is the official identifier MCAZ uses for this instrument.
- Instrument
- SR
- Full name
- SR 03 Rev 7
- Category
- Registration
- Authority source
- English
- Readable HTML
- 0 articles · 1 language version
- Published
- —
- Effective
- 2020-10-01
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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.
Sample Receipt Form - Medical Devices
SR 03 Rev 7, the Samples Repository Office's controlled receipt form for medical device samples, footered "Rev 7_October 2020" on every page. It is a BLANK form, not an instrument: Part A takes the customer details, Part B the product details (classification, brand and type, manufacturer, country of origin, licence number, package size), Part C the terms and conditions under which the MCAZ laboratory accepts and handles a submitted sample — including its confidentiality undertakings and the process requirements where a statement of conformity is requested — and Part D is the MCAZ-use-only receipt and forwarding record. It is ingested as `form-instructions` because that is what it is: the completion requirements for a prescribed form, which is the one part of it that carries regulatory content. Round 207 flagged this document as a judgement call ("flip to not-a-document if the corpus is to hold instruments only"); the call taken here is to ingest it, because its terms and conditions are substantive text a submitter is bound by, and its row says plainly that it is a form.
SR 03 Rev 7 is the official identifier MCAZ uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.