ATELLICA IM FOLITROPINA (FSH)
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered January 29, 2019ENSAYO PARA LA DETERMINACION DE FOLITROPINA
ASSAY FOR THE DETERMINATION OF FOLLITROPIN
- 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 FOLITROPINA
- Trade Name (English)
- ASSAY FOR THE DETERMINATION OF FOLLITROPIN
- Analysis ID
- 116R2019 SSA
- Registration Date
- January 29, 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 ATELLICA IM FOLITROPINA (FSH) (ATELLICA IM FOLITROPINA (FSH)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 116R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on January 29, 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.