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SONDAS LÁSER BAUSCH & LOMB - COFEPRIS Registration 262E2019 SSA

Access comprehensive regulatory information for SONDAS LÁSER BAUSCH & LOMB (BAUSCH & LOMB LASER PROBES) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 262E2019 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on February 12, 2019.

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.

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COFEPRIS Official Data
Clase II
262E2019 SSA
SONDAS LÁSER BAUSCH & LOMB
COFEPRIS Analysis ID: 262E2019 SSA
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Product Use / Uso del Producto
Spanish

LAS SONDAS LÁSER RECTA O CURVA, ESTÉRILES DESECHABLES ESTÁN INDICADAS PARA LA FOTOCOAGULACIÓN DURANTE LA CIRUGÍA OFTÁLMICA. CIERTOS MODELOS TIENEN CARACTERÍSTICAS ADICIONALES PARA PROPORCIONAR UNA FUNCIÓN DE ILUMINACIÓN O ASPIRACIÓN. EL DISPOSITIVO ESTÁ C

English

DISPOSABLE STRAIGHT OR CURVED, STERILE LASER PROBES ARE INDICATED FOR PHOTOCOAGULATION DURING OPHTHALMIC SURGERY. CERTAIN MODELS HAVE ADDITIONAL FEATURES TO PROVIDE A LIGHTING OR VACUUM FUNCTION. THE DEVICE IS C

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
SONDAS LÁSER
Trade Name (English)
LASER PROBES
Registration Information
Analysis ID
262E2019 SSA
Registration Date
February 12, 2019
Manufacturer / Fabricante
Name (English)
BAUSCH & LOMB MÉXICO, S.A. DE C.V.