MFDS 의료기기법의료기기법 시행규칙 [별지 제31호서식]
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
의료기기법 시행규칙 [별지 제31호서식] is the official MFDS identifier for “Medical-device product change certification application — Enforcement Rule Form 31”. 의료기기법 시행규칙 [별지 제31호서식] is the official identifier MFDS uses for this instrument.
- Instrument
- 의료기기법
- Full name
- 의료기기법 시행규칙 [별지 제31호서식]
- Category
- Registration
- Source publication
- Korean
- Readable HTML
- 1 language version
- Published
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- 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.
Medical-device product change certification application — Enforcement Rule Form 31
Complete two-page official change certification form, marked amended 31 December 2020. Preserves the NIDS addressee, printed period, conditional dossier, distinct electronic and visit/post fee columns and reverse-side administrative-sanction transfer acknowledgement. Parent-rule consolidation dates are not substituted for this form amendment date. Original full-page images govern; native text is an explicitly incomplete search layer. Source preservation does not establish current legal effect or whole-country completeness.
의료기기법 시행규칙 [별지 제31호서식] is the official identifier MFDS uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.