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THE UNFOLDER PLATINUM 1 SERIES CARTRIDGE - COFEPRIS Registration 1347E2019 SSA

Access comprehensive regulatory information for THE UNFOLDER PLATINUM 1 SERIES CARTRIDGE (THE UNFOLDER PLATINUM 1 SERIES CARTRIDGE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1347E2019 SSA and manufactured by JOHNSON & JOHNSON DE Mร‰XICO, S.A. DE C.V.. The device was registered on July 16, 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
1347E2019 SSA
THE UNFOLDER PLATINUM 1 SERIES CARTRIDGE
COFEPRIS Analysis ID: 1347E2019 SSA
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Product Use / Uso del Producto
Spanish

PARA PLEGAR Y ASISTIR EN LA INSERCIร“N DE LAS LENTES INTRAOCULARES ACRรLICAS DE UNA PIEZA AMO DENTRO DEL OJO.

English

TO FOLD AND ASSIST IN THE INSERTION OF ACRYLIC INTRAOCULAR LENSES OF A MASTER PIECE INSIDE THE EYE.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO Mร‰DICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
CARTUCHO PARA INTRODUCCIร“N DE LENTES INTRAOCULARES
Trade Name (English)
CARTRIDGE FOR INSERTION OF INTRAOCULAR LENSES
Registration Information
Analysis ID
1347E2019 SSA
Registration Date
July 16, 2019
Manufacturer / Fabricante
Name (English)
JOHNSON & JOHNSON DE Mร‰XICO, S.A. DE C.V.