CK MB LIQUID
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered December 03, 2019ENSAYO PARA LA DETERMINACION DE CK MB LIQUIDA
TEST FOR THE DETERMINATION OF CK MB LIQUID
- 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 LA DETERMINACION DE CK MB LIQUIDA
- Trade Name (English)
- TEST FOR THE DETERMINATION OF CK MB LIQUID
- Analysis ID
- 2202R2019 SSA
- Registration Date
- December 03, 2019
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR
Access comprehensive regulatory information for CK MB LIQUID (CK MB LIQUID) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2202R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on December 03, 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.