PRUEBA RÁPIDA CUANTITATIVA PCT
Mexico·Clase I·III. Agentes de diagnóstico·EMERGO, S. DE R.L.
DE C.V.·Registered October 19, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- PRUEBA RÁPIDA PCT BIOTIME
- Trade Name (English)
- PRUEBA RÁPIDA PCT BIOTIME
- Analysis ID
- 1095R2022 SSA
- Registration Date
- October 19, 2022
- Name (Spanish)
- EMERGO, S. DE R.L. DE C.V.
- Name (English)
- EMERGO, S. DE R.L. DE C.V.
Access comprehensive regulatory information for PRUEBA RÁPIDA CUANTITATIVA PCT (PRUEBA RÁPIDA CUANTITATIVA PCT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1095R2022 SSA and manufactured by EMERGO, S. DE R.L. DE C.V.. The device was registered on October 19, 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.