BLOOD GAS CONTROL LEVEL 1, 2 & 3 (BG CONTROL 1, 2 & 3)
ESTE PRODUCTO ESTÁ DESTINADO PARA USO DE DIAGNÓSTICO IN VITRO, EN EL CONTROL DE CALIDAD DEL ANÁLISIS DE GAS DE SANGRE.
THIS PRODUCT IS INTENDED FOR IN VITRO DIAGNOSTIC USE, IN THE QUALITY CONTROL OF BLOOD GAS ANALYSIS.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- CONTROL DE CALIDAD
- Trade Name (English)
- QUALITY CONTROL
- Analysis ID
- 1991R2018 SSA
- Registration Date
- August 10, 2018
- Name (English)
- INTEGRAL SOLUTION TO YOUR REGULATORY NEEDS, S.A. DE C.V.
Access comprehensive regulatory information for BLOOD GAS CONTROL LEVEL 1, 2 & 3 (BG CONTROL 1, 2 & 3) (BLOOD GAS CONTROL LEVEL 1, 2 & 3 (BG CONTROL 1, 2 & 3)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1991R2018 SSA and manufactured by SOLUCIÓN INTEGRAL A SUS NECESIDADES REGULATORIAS, S.A. DE C.V.. The device was registered on August 10, 2018.
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.