DLSMI DocumentMedical-device registration application — Annex 1 (Russian)
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Заявление о проведении регистрации 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.
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- Document
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- Medical-device registration application — Annex 1 (Russian)
- Category
- Registration
- Source publication
- Russian
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Заявление о проведении регистрации медицинского изделия
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 Russian header attributes the order to the Ministry of Health, while other annex headers name DLSMI; the issuer discrepancy is unresolved.
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.