MICROPURE.
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·ARFAMEX, S.A. DE C.V.·Registered January 15, 2018LENTES INTRAOCULARES DE CÁMARA POSTERIOR, INDICADOS PARA EL REEMPLAZO DEL CRISTALINO HUMANO PARA LOGRAR LA CORRECCIÓN VISUAL DE AFAQUIA EN PACIENTES ADULTOS DESPUÉS DE LA CIRUGÍA DE CATARATAS.
POSTERIOR CHAMBER INTRAOCULAR LENSES, INDICATED FOR THE REPLACEMENT OF THE HUMAN LENS TO ACHIEVE VISUAL CORRECTION OF APHAKIA IN ADULT PATIENTS AFTER CATARACT SURGERY.
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
- Product Type (English)
- II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- IMPLANTE - LENTE INTROCULAR.
- Trade Name (English)
- IMPLANT - INTROCULAR LENS.
- Analysis ID
- 185C2018 SSA
- Registration Date
- January 15, 2018
- Name (Spanish)
- ARFAMEX, S.A. DE C.V.
- Name (English)
- ARFAMEX, S.A. DE C.V.
Access comprehensive regulatory information for MICROPURE. (MICROPURE.) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 185C2018 SSA and manufactured by ARFAMEX, S.A. DE C.V.. The device was registered on January 15, 2018.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.