VIBEX PARACEL.
Mexico·Clase II·V. SURGICAL AND HEALING MATERIALS·ARFAMEX, S.A. DE C.V.·Registered January 15, 2018PARA EL ENDURECIMIENTO CORNEAL, DESPUÉS DE REMOVER EL EPITELIO O SOBRE LA BASE DE ESTROMA. EXCLUSÍVAMENTE PARA USO OFTÁLMICO, NO INYECTAR.
FOR CORNEAL HARDENING, AFTER REMOVING THE EPITHELIUM OR ON THE STROMAL BASIS. EXCLUSIVELY FOR OPHTHALMIC USE, DO NOT INJECT.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
- Product Type (English)
- V. SURGICAL AND HEALING MATERIALS
- Trade Name (Spanish)
- RIBOFLAVINA PARA USO OFTÁLMICO.
- Trade Name (English)
- RIBOFLAVIN FOR OPHTHALMIC USE.
- Analysis ID
- 187C2018 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 VIBEX PARACEL. (VIBEX PARACEL.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 187C2018 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 (V. SURGICAL AND HEALING MATERIALS), 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.