PRUEBA RÁPIDA DE UN SOLO PASO PARA LA DETECCIÓN CUALITATIVA DE SANGRE HUMANA EN HECES
Mexico·Clase I·III. Agentes de diagnóstico·ABBOTT
LABORATORIES DE
MÉXICO, S.A. DE C.V.·Registered December 09, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- FOB ONE STEP FECAL OCCULT BLOOD TEST DEVICE (FECES)
- Trade Name (English)
- FOB ONE STEP FECAL OCCULT BLOOD TEST DEVICE (FECES)
- Analysis ID
- 1555R2022 SSA
- Registration Date
- December 09, 2022
- 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 PRUEBA RÁPIDA DE UN SOLO PASO PARA LA DETECCIÓN CUALITATIVA DE SANGRE HUMANA EN HECES (PRUEBA RÁPIDA DE UN SOLO PASO PARA LA DETECCIÓN CUALITATIVA DE SANGRE HUMANA EN HECES) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1555R2022 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on December 09, 2022.
This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.