URIC ACID2
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.·Registered August 08, 2022ENSAYOPARALADETERMINACIÓNCUANTITATIVADEÁCIDOÚRICO
ASSAY for the quantitative determination of uric acid
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO PARA LADETERMINACIÓN CUANTITATIVA DE ÁCIDO ÚRICO
- Trade Name (English)
- ASSAY FOR THE QUANTITATIVE DETERMINATION OF URIC ACID
- Analysis ID
- 0734R2022 SSA
- Registration Date
- August 08, 2022
- Name (Spanish)
- ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTTLABORATORIES DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for URIC ACID2 (URIC ACID2) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0734R2022 SSA and manufactured by ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on August 08, 2022.
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.