DLSMI DocumentMedical-device corrective safety action report form — Annex 8 (Russian)
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Форма отчета о корректирующих действиях по безопасности медицинского изделия is published by Department of Medicines and Medical Devices, Ministry of Health. This document is identified by its title; no separate official document code is recorded.
- Instrument
- Document
- Full name
- Medical-device corrective safety action report form — Annex 8 (Russian)
- Category
- Vigilance
- Source publication
- Russian
- Readable HTML
- 1 language version
- Published
- —
- Effective
- —
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Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Форма отчета о корректирующих действиях по безопасности медицинского изделия
Manufacturer/authorized representative corrective safety action report;initial/follow-up/final;device/GMDN/UDI/risk,FSCA reasons/actions/schedule,attachment of safety notice in Russian;mandatory-field legends1/2/3. Field legends distinguish report stages; conditional GMDN/UDI/risk fields are not universal requirements for every device. The source header refers to order 299 dated 30 September 2024; the signed parent order and current amendment chain remain unverified. No publication or effective date is inferred from that reference or Office metadata.
This document is identified by its title; no separate official document code is recorded. Always confirm the current consolidated text and transition provisions with the official source before filing.