DISPOSITIVO AUTOMATIZADO DE LOCALIZACIÓN CELULAR
Mexico·Clase I·I. Equipo Médico·ABBOTT
LABORATORIES DE
MÉXICO, S.A. DE C.V.·Registered December 07, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- I. Equipo Médico
- Product Type (English)
- I. Equipo Médico
- Trade Name (Spanish)
- CELLAVISION® DM 1200
- Trade Name (English)
- CELLAVISION® DM 1200
- Analysis ID
- 1538E2022 SSA
- Registration Date
- December 07, 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 DISPOSITIVO AUTOMATIZADO DE LOCALIZACIÓN CELULAR (DISPOSITIVO AUTOMATIZADO DE LOCALIZACIÓN CELULAR) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1538E2022 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on December 07, 2022.
This page provides complete registration details including product type (I. Equipo Médico), 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.