Mexico COFEPRIS registration 0812E2024 SSA
CÁMARA DE FONDO DE OJO
EN: CÁMARA DE FONDO DE OJO
Device classification
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. Equipo Médico
- Product Type (English)
- I. Equipo Médico
- Trade Name (Spanish)
- FUNDUS CAMERA
- Trade Name (English)
- FUNDUS CAMERA
Registration information
- Analysis ID
- 0812E2024 SSA
- Registration Date
- March 22, 2024
Manufacturer / Fabricante
- Name (Spanish)
- ARFAMEX, S.A. DE C.V.
- Name (English)
- ARFAMEX, S.A. DE C.V.
About this record
Access comprehensive regulatory information for CÁMARA DE FONDO DE OJO (CÁMARA DE FONDO DE OJO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0812E2024 SSA and manufactured by ARFAMEX, S.A. DE C.V.. The device was registered on March 22, 2024.
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.
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