PSA ELISA CALBIOTECH
Mexico·Clase I·III. DIAGNOSTIC AGENTS·QUIMIBIOL, S.A. DE C.V.·Registered September 10, 2019INMUNOENSAYO PARA LA CUANTIFICACIÓN DE TIROXINA LIBRE EN SUERO O PLASMA.
IMMUNOASSAY FOR THE QUANTIFICATION OF FREE THYROXINE IN SERUM OR PLASMA.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA PARA DETERMINAR ANTÍGENO PROSTÁTICO (PSA)
- Trade Name (English)
- TEST TO DETERMINE PROSTATE ANTIGEN (PSA)
- Analysis ID
- 1829R2019 SSA
- Registration Date
- September 10, 2019
- Name (Spanish)
- QUIMIBIOL, S.A. DE C.V.
- Name (English)
- QUIMIBIOL, S.A. DE C.V.
Access comprehensive regulatory information for PSA ELISA CALBIOTECH (PSA ELISA CALBIOTECH) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1829R2019 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on September 10, 2019.
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.