DLSMI DocumentMedical-device postregistration clinical monitoring report form — Annex 9 (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 9. Медициналык буюмдун коопсуздугуна жана натыйжалуулугуна каттоодон кийинки клиникалык мониторинг тууралуу отчету 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.
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- Medical-device postregistration clinical monitoring report form — Annex 9 (Kyrgyz)
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- Vigilance
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- Kyrgyz
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Тиркеме 9. Медициналык буюмдун коопсуздугуна жана натыйжалуулугуна каттоодон кийинки клиникалык мониторинг тууралуу отчету формасы
Postregistration clinical monitoring report;17 sections;class3 nonimplantable/implantable and implanted class2b choices;residual risks,clinical data,plan adjustment,FSCA,cycle extension. Class 3 nonimplantable/implantable and implanted class 2b choices are preserved; this form is not evidence of a blanket monitoring obligation for all devices or IVDs. 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.