Pure Global

VIBEX PARACEL. - COFEPRIS Registration 187C2018 SSA

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.

Free Database
Powered by Pure Global AI
COFEPRIS Official Data
Clase II
187C2018 SSA
VIBEX PARACEL.
COFEPRIS Analysis ID: 187C2018 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

PARA EL ENDURECIMIENTO CORNEAL, DESPUÉS DE REMOVER EL EPITELIO O SOBRE LA BASE DE ESTROMA. EXCLUSÍVAMENTE PARA USO OFTÁLMICO, NO INYECTAR.

English

FOR CORNEAL HARDENING, AFTER REMOVING THE EPITHELIUM OR ON THE STROMAL BASIS. EXCLUSIVELY FOR OPHTHALMIC USE, DO NOT INJECT.

Device Classification
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.
Registration Information
Analysis ID
187C2018 SSA
Registration Date
January 15, 2018
Manufacturer / Fabricante
Name (Spanish)
ARFAMEX, S.A. DE C.V.
Name (English)
ARFAMEX, S.A. DE C.V.