ALINITY I DHEA-S
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.·Registered November 27, 2019ENSAYO PARA LA DETERMINACIÓN CUANTITATIVA DE SULFATO DE DESHIDROEPIANDROSTERONA (DHEA-S)
TEST FOR THE QUANTITATIVE DETERMINATION OF DEHYDROEPIANDROSTERONE SULPHATE (DHEA-S)
- 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 DETERMINACIÓN CUANTITATIVA DE SULFATO DE DESHIDROEPIANDROSTERONA (DHEA-S)
- Trade Name (English)
- TEST FOR THE QUANTITATIVE DETERMINATION OF DEHYDROEPIANDROSTERONE SULPHATE (DHEA-S)
- Analysis ID
- 2196R2019 SSA
- Registration Date
- November 27, 2019
- Name (Spanish)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for ALINITY I DHEA-S (ALINITY I DHEA-S) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2196R2019 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on November 27, 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.