DLSMI DocumentMedical-device incident report form — Annex 7 (Kyrgyz)
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Тиркеме 7. Медициналык буюмдун жагымсыз окуя (инцидент) жөнүндө отчеттун формасы 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 incident report form — Annex 7 (Kyrgyz)
- Category
- Vigilance
- Source publication
- Kyrgyz
- Readable HTML
- 1 language version
- Published
- —
- Effective
- —
Open a language version
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.
Тиркеме 7. Медициналык буюмдун жагымсыз окуя (инцидент) жөнүндө отчеттун формасы
Manufacturer/authorized representative incident report;initial/follow-up/final;device/GMDN/UDI/risk,incident,patient,healthcare organization,initial analysis and final investigation;mandatory-field legends1/2/3. Field legends distinguish initial, follow-up and final reports; 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.