Mexico COFEPRIS registration 1673R2022 SSA
CALIBRADOR.
EN: CALIBRADOR.
Device classification
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- CALIBRATOR FOR AUTOMATED SYSTEMS ROCHE.
- Trade Name (English)
- CALIBRATOR FOR AUTOMATED SYSTEMS ROCHE.
Registration information
- Analysis ID
- 1673R2022 SSA
- Registration Date
- December 16, 2022
Manufacturer / Fabricante
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
About this record
Access comprehensive regulatory information for CALIBRADOR. (CALIBRADOR.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1673R2022 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on December 16, 2022.
This page provides complete registration details including product type (III. Agentes de diagnóstico), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
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