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COFEPRIS Document

COFEPRIS Class I, II and III medical-device registration guide

Guía para la obtención del registro sanitario de dispositivos médicos Clase I, II y III
MexicoComisión Federal para la Protección contra Riesgos SanitariosRegistrationCurrentness under review
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Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.

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Guía para la obtención del registro sanitario de dispositivos médicos Clase I, II y III is published by Comisión Federal para la Protección contra Riesgos Sanitarios. This document is identified by its title; no separate official document code is recorded.

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COFEPRIS Class I, II and III medical-device registration guide
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Registration
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About this regulation

Guía para la obtención del registro sanitario de dispositivos médicos Clase I, II y III

Complete captured official 62-page COFEPRIS guide for initial registration of Class I, II and III medical devices, including software-as-device dossier checklists. All original physical page images are mandatory and authoritative; exact native text is explicitly incomplete search text and may contain extraction artifacts or omit image words. This source is distinct from post-approval modification and grouping rules; references to FEUM do not reproduce or replace final Appendix III.3 or IV. Source currentness is unverified.

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.