VISCOJECT™ BIO 1.8
Mexico·Clase II·I. MEDICAL EQUIPMENT·BAUSCH & LOMB MÉXICO, S.A. DE C.V.·Registered August 27, 2018SISTEMA DE INYECCIÓN DE LENTES DE UN SOLO USO PARA LA INYECCIÓN DE LENTES INTRAOCULARES PLEGABLES DE ACRÍLICO DE UNA PIEZA.
SINGLE-USE LENS INJECTION SYSTEM FOR THE INJECTION OF ONE-PIECE ACRYLIC FOLDING INTRAOCULAR LENSES.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- SISTEMA DE INYECCIÓN DE LENTES.
- Trade Name (English)
- LENS INJECTION SYSTEM.
- Analysis ID
- 2078E2018 SSA
- Registration Date
- August 27, 2018
- Name (Spanish)
- BAUSCH & LOMB MÉXICO, S.A. DE C.V.
- Name (English)
- BAUSCH & LOMB MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for VISCOJECT™ BIO 1.8 (VISCOJECT™ ORGANIC 1.8) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2078E2018 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on August 27, 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.