DLSMI DocumentMedical-device registration application — Annex 1 (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 1. Медициналык буюмдарга каттоо жүргүзүү жөнүндө Арыз 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 registration application — Annex 1 (Kyrgyz)
- Category
- Registration
- 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 1. Медициналык буюмдарга каттоо жүргүзүү жөнүндө Арыз
Device-registration application: product, intended use/field, risk/GMDN, drug component, configuration, storage, foreign registrations, manufacture and authorized representative; guarantee/signature. The GMDN field is conditional (if available); no universal GMDN submission obligation is inferred. 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.