Pure Global

DYNAMESH ENDOLAP - COFEPRIS Registration 642C2021 SSA

Access comprehensive regulatory information for DYNAMESH ENDOLAP (DYNAMESH ENDOLAP) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 642C2021 SSA and manufactured by ISA HEALTH S.A. DE C.V.. The device was registered on April 13, 2021.

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 III
642C2021 SSA
DYNAMESH ENDOLAP
COFEPRIS Analysis ID: 642C2021 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

MALLA QUIRรšRGICA PARA HERNIAABDOMINAL POLIMERO SINTETICO NOBIOABSORBIBLE

English

SURGICAL MESH FOR ABDOMINAL HERNIAABDOMINAL NONBIOABSORBABLE SYNTHETIC POLYMER

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
V. MATERIALES QUIRรšRGICOS Y DE CURACIร“N
Product Type (English)
V. SURGICAL AND HEALING MATERIALS
Trade Name (Spanish)
MALLA QUIRรšRGICA PARA HERNIAABDOMINAL POLIMERO SINTETICO NOBIOABSORBIBLE
Trade Name (English)
SURGICAL MESH FOR ABDOMINAL HERNIAABDOMINAL NONBIOABSORBABLE SYNTHETIC POLYMER
Registration Information
Analysis ID
642C2021 SSA
Registration Date
April 13, 2021
Manufacturer / Fabricante
Name (English)
ISA HEALTH S.A. DE C.V.