KIT DE ENSAYO PARA LA DETERMINACIÓN IN VITRO CUALITATIVA DE ANTICUERPOS IGG PARA EL DIAGNÓSTICO DE CHLAMYDIA TRACHOMATIS
Mexico·Clase II·III. Agentes de diagnóstico·INOCHEM, S.A. DE
C.V.·Registered December 16, 2022- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- ANTI-CHLAMYDIA TRACHOMATIS EUROLINE-WB (IGG)
- Trade Name (English)
- ANTI-CHLAMYDIA TRACHOMATIS EUROLINE-WB (IGG)
- Analysis ID
- 1651R2022 SSA
- Registration Date
- December 16, 2022
- Name (Spanish)
- INOCHEM, S.A. DE C.V.
- Name (English)
- INOCHEM, S.A. DE C.V.
Access comprehensive regulatory information for KIT DE ENSAYO PARA LA DETERMINACIÓN IN VITRO CUALITATIVA DE ANTICUERPOS IGG PARA EL DIAGNÓSTICO DE CHLAMYDIA TRACHOMATIS (KIT DE ENSAYO PARA LA DETERMINACIÓN IN VITRO CUALITATIVA DE ANTICUERPOS IGG PARA EL DIAGNÓSTICO DE CHLAMYDIA TRACHOMATIS) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1651R2022 SSA and manufactured by INOCHEM, 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.