CYSC2
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DEC.V.·Registered December 04, 2020REACTIVO DE DIAGNÓSTICO IN VITRO PARACISTATINA C
IN VITRO PARACIST DIAGNOSTIC REAGENT C
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVODEDIAGNÓSTICOINVITROPARA CISTATINA C
- Trade Name (English)
- REACTIVODEDIAGNÓSTICOINVITROPARA CISTATINA C
- Analysis ID
- 1615R2020 SSA
- Registration Date
- December 04, 2020
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DEC.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DEC.V.
Access comprehensive regulatory information for CYSC2 (CYSC2) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1615R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on December 04, 2020.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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.