ELECSYS HGH
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DE C.V.·Registered October 07, 2019PRUEBA IN VITRO PARA LA DETERMINACIÓN CUANTITATIVA DE LA HORMONA DEL CRECIMIENTO HUMANO EN SUERO Y PLASMA HUMANOS.
IN VITRO TEST FOR THE QUANTITATIVE DETERMINATION OF HUMAN GROWTH HORMONE IN HUMAN SERUM AND PLASMA.
- 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 DETERMINACIÓN DE LA HORMONA DEL CRECIMIENTO HUMANO (HGH)
- Trade Name (English)
- TEST FOR THE DETERMINATION OF HUMAN GROWTH HORMONE (HGH)
- Analysis ID
- 1951R2019 SSA
- Registration Date
- October 07, 2019
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
Access comprehensive regulatory information for ELECSYS HGH (ELECSYS HGH) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1951R2019 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on October 07, 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.