SILICONE GEL IN TUBE - ANVISA Registration 80153820021

Access comprehensive regulatory information for SILICONE GEL IN TUBE in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80153820021 and manufactured by IMPLANTECH ASSOCIATES, INC. The registration is held by TG MED COMERCIO IMPORTACAO, EXPORTACAO, FABRICACAO E DISTRIBUICAO DE PRODUTOS MEDICOS 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 FRESCO INTERNATIONAL 2005, SA, EUROFARMA LABORATÓRIOS S.A, 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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80153820021
Registration Details
ANVISA Registration Number: 80153820021
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

CIMEOSIL® SCAR AND LASER GEL
Risk Class I

Registration Details

80153820021

25351515545202019

04058136000103

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 03, 2020

VIGENTE

09/18/2025 19:00:01