Post-Surgical Mesh - ANVISA Registration 80674930018

Access comprehensive regulatory information for Post-Surgical Mesh in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80674930018 and manufactured by TYTEX A/S. The registration is held by GCA BRASIL IMPORTACAO E EXPORTACAO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOA FORMA CONFECÇÕES LTDA, Plie ConfecçÔes Ltda, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80674930018
Registration Details
ANVISA Registration Number: 80674930018
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

đŸ‡§đŸ‡· Brazil Regulatory Expert

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Device Details

Registration Details

80674930018

25351264749202329

11015655000150

Company Information

TYTEX A/S
Denmark
PT: DINAMARCA

Dates and Status

May 15, 2023

VIGENTE

09/18/2025 19:00:01