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Dilatation Balloons - ANVISA Registration 10334789011

Access comprehensive regulatory information for Dilatation Balloons in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10334789011 and manufactured by DIVERSATEK HEALTHCARE INC.. The registration is held by G.F.E. DO BRASIL LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including E-MED PRODUTOS Mร‰DICO-HOSPITALARES LTDA - ME, MEDTEC SUPPLIES, INDUSTRIA, IMPORTACAO, EXPORTACAO, DISTRIBUICAO E COMERCIO 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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10334789011
Registration Details
ANVISA Registration Number: 10334789011
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Device Details

BALรƒO DILATADOR - VIPER
Risk Class I

Registration Details

10334789011

25351371589202454

55126981000100

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Jul 22, 2024

VIGENTE

09/18/2025 19:00:01