EMIT II PLUS 6-ACETYLMORPHINE ASSAY
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered March 07, 2018REACTIVO PARA LA DETERMINACION DE 6-ACETILMORFINA
REAGENT FOR THE DETERMINATION OF 6-ACETHYLMORPHINE
- 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 6-ACETILMORFINA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF 6-ACETHYLMORPHINE
- Analysis ID
- 679R2018 SSA
- Registration Date
- March 07, 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 EMIT II PLUS 6-ACETYLMORPHINE ASSAY (EMIT II PLUS 6-ACETYLMORPHINE ASSAY) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 679R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on March 07, 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.