FLUID PACK 0018165300
Mexico·Clase I·III. DIAGNOSTIC AGENTS·I.L. DIAGNOSTICS, S.A. DE C.V.·Registered October 29, 2020FLUIDPACKSEUTILIZAPARALACALIBRACIÓNDE SODIO, POTASIO Y CLORURO UTILIZANDOLOS ANALIZADORES DE QUÍMICA CLÍNICA ILAB.
FLUIDPACK IS USED FOR SODIUM, POTASSIUM AND CHLORIDE CALIBRATION USING ILAB CLINICAL CHEMISTRY ANALYZERS.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- CALIBRADOR
- Trade Name (English)
- CALIBRADOR
- Analysis ID
- 1487R2020 SSA
- Registration Date
- October 29, 2020
- Name (Spanish)
- I.L. DIAGNOSTICS, S.A. DE C.V.
- Name (English)
- I.L. DIAGNOSTICS, S.A. DE C.V.
Access comprehensive regulatory information for FLUID PACK 0018165300 (FLUID PACK 0018165300) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1487R2020 SSA and manufactured by I.L. DIAGNOSTICS, S.A. DE C.V.. The device was registered on October 29, 2020.
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.