MYOGLOBIN (MYO) TEST KIT (IMMUNOFLUORESCENCE)
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ATYDE MÉXICO S.A. DE C.V.·Registered December 13, 2019REACTIVOS PARA DETECCIÓN DE PROCALCITONINA (PCT)
PROCALCITONIN DETECTION REAGENTS (PCT)
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVOS PARA DETECCIÓN DE PROCALCITONINA (PCT)
- Trade Name (English)
- PROCALCITONIN DETECTION REAGENTS (PCT)
- Analysis ID
- 2264R2019 SSA
- Registration Date
- December 13, 2019
- Name (Spanish)
- ATYDE MÉXICO S.A. DE C.V.
- Name (English)
- ATYDE MEXICO S.A. DE C.V.
Access comprehensive regulatory information for MYOGLOBIN (MYO) TEST KIT (IMMUNOFLUORESCENCE) (MYOGLOBIN (MYO) TEST KIT (IMMUNOFLUORESCENCE)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2264R2019 SSA and manufactured by ATYDE MÉXICO S.A. DE C.V.. The device was registered on December 13, 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.