URIDIAG.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·QUIMIBIOL, S.A. DE C.V.·Registered October 25, 2019TIRAS REACTIVAS DE URIANÁLISIS. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETE.
URINALYSIS TEST STRIPS. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR USE IN CLINICAL OR CABINET LABORATORIES ONLY.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- TIRAS REACTIVAS.
- Trade Name (English)
- TEST STRIPS.
- Analysis ID
- 2041R2019 SSA
- Registration Date
- October 25, 2019
- Name (Spanish)
- QUIMIBIOL, S.A. DE C.V.
- Name (English)
- QUIMIBIOL, S.A. DE C.V.
Access comprehensive regulatory information for URIDIAG. (URIDIAG.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2041R2019 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on October 25, 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.