ANKORIS.
Mexico·Clase III·I. MEDICAL EQUIPMENT·ARFAMEX, S.A. DE C.V.·Registered January 09, 2018PARA LA ESTABILIDAD ROTACIONAL Y LIMITAR EL DESPLAZAMIENTO HORIZONTAL / VERTICAL DE LA IOL EN EL OJO.
FOR ROTATIONAL STABILITY AND LIMIT THE HORIZONTAL/VERTICAL DISPLACEMENT OF THE IOL IN THE EYE.
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- IMPLANTE - LENTE INTRAOCULAR.
- Trade Name (English)
- IMPLANT - INTRAOCULAR LENS.
- Analysis ID
- 155E2018 SSA
- Registration Date
- January 09, 2018
- Name (Spanish)
- ARFAMEX, S.A. DE C.V.
- Name (English)
- ARFAMEX, S.A. DE C.V.
Access comprehensive regulatory information for ANKORIS. (ANKORIS.) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 155E2018 SSA and manufactured by ARFAMEX, S.A. DE C.V.. The device was registered on January 09, 2018.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.