DS- I (NO. 3)
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ATYDE MÉXICO, S.A. DE C.V.·Registered October 25, 2018KIT DE REACTIVOS PARA SER UTILIZADO EN ANALIZADORES DE ELECTROLITOS PARA LA DETERMINACIÓN DE POTASIO (K+), SODIO (NA+), CLORURO (CL-), CALCIO (CA2+), LITIO (LI+), PH (VALOR DE PH) Y TCO2 EN SUERO HUMANO.
KIT OF REAGENTS TO BE USED IN ELECTROLYTE ANALYZERS FOR THE DETERMINATION OF POTASSIUM (K+), SODIUM (NA+), CHLORIDE (CL-), CALCIUM (CA2+), LITHIUM (LI+), PH (PH VALUE) AND TCO2 IN HUMAN SERUM.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- KIT PARA LA DETERMINACIÓN DE POTASIO, SODIO, CLORURO, CALCIO, LITIO, PH Y TCO2 EN SUERO HUMANO.
- Trade Name (English)
- KIT FOR THE DETERMINATION OF POTASSIUM, SODIUM, CHLORIDE, CALCIUM, LITHIUM, PH AND TCO2 IN HUMAN SERUM.
- Analysis ID
- 2462R2018 SSA
- Registration Date
- October 25, 2018
- Name (Spanish)
- ATYDE MÉXICO, S.A. DE C.V.
- Name (English)
- ATYDE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for DS- I (NO. 3) (SAT- I (NO. 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 2462R2018 SSA and manufactured by ATYDE MÉXICO, S.A. DE C.V.. The device was registered on October 25, 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.