IMMULITE®/ IMMULITE® 1000 SYSTEMS PROGESTERONE.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered March 12, 2018REACTIVO PARA LA DETERMINACION DE PROGESTERONA
REAGENT FOR THE DETERMINATION OF PROGESTERONE
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVO PARA LA DETERMINACION DE PROGESTERONA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF PROGESTERONE
- Analysis ID
- 750R2018 SSA
- Registration Date
- March 12, 2018
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR
Access comprehensive regulatory information for IMMULITE®/ IMMULITE® 1000 SYSTEMS PROGESTERONE. (IMMULITE®/ IMMULITE® 1000 SYSTEMS PROGESTERONE.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 750R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on March 12, 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.