NEPHSTAR C1 INACTIVADOR KIT
LA PRUEBA SE UTILIZA PARA LADETERMINACIÓN CUANTITATIVA DELINACTIVADOR C1 HUMANO EN SUERO COMOAYUDAENELDIAGNÓSTICODELMETABOLISMOANORMAL DE C1IN
THE TEST IS USED FOR THE QUANTITATIVE DETERMINATION OF HUMAN C1 ACTIVATOR IN SERUM AS AN AID IN THE DIAGNOSIS OF NORMAL C1IN METABOLISM
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA PARA LA DETERMINACIÓNDEL INACTIVADOR C1 (C1IN)
- Trade Name (English)
- TEST FOR THE DETERMINATION OF THE INACTIVATOR C1 (C1IN)
- Analysis ID
- 1246R2020 SSA
- Registration Date
- September 11, 2020
- Name (Spanish)
- KABLA COMERCIAL, S.A. DEC.V.
- Name (English)
- KABBALAH COMMERCIAL, S.A. DEC.V.
Access comprehensive regulatory information for NEPHSTAR C1 INACTIVADOR KIT (NEPHSTAR C1 INACTIVADOR KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1246R2020 SSA and manufactured by KABLA COMERCIAL, S.A. DEC.V.. The device was registered on September 11, 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.