Mexico COFEPRIS registration 955E2019 SSA

VIPER PRIMETM INSTRUMENTS

EN: VIPER PRIMETM INSTRUMENTS
Mexico flagMexico·Clase I·I. MEDICAL EQUIPMENT·JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.·Registered May 09, 2019
Product Use / Uso del Producto
Spanish

LOS INSTRUMENTOS PARA TEJIDO NEURAL DE DEPUY SYNTHES ESTÁN INDICADOS PARA UTILIZARSE ÚNICAMENTE EN EL SISTEMA NERVIOSO PERIFÉRICO. LOS INSTRUMENTOS PARA TEJIDO NEURAL SON HERRAMIENTAS DISEÑADAS PARA QUE LAS USEN LOS CIRUJANOS EN INTERVENCIONES DE COLUMNA,

English

DEPUY SYNTHES NEURAL TISSUE INSTRUMENTS ARE INTENDED FOR USE IN THE PERIPHERAL NERVOUS SYSTEM ONLY. NEURAL TISSUE INSTRUMENTS ARE TOOLS DESIGNED FOR USE BY SURGEONS IN SPINAL INTERVENTIONS,

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
INSTRUMENTAL QUIRURGICO
Trade Name (English)
SURGICAL INSTRUMENTS
Registration information
Analysis ID
955E2019 SSA
Registration Date
May 09, 2019
Manufacturer / Fabricante
Name (English)
JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.
About this record

Access comprehensive regulatory information for VIPER PRIMETM INSTRUMENTS (VIPER PRIMETM INSTRUMENTS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 955E2019 SSA and manufactured by JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.. The device was registered on May 09, 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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