Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Dilators - ANVISA Registration 81042210003

Access comprehensive regulatory information for Dilators in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81042210003 and manufactured by GTA SRL. The registration is held by Porto71 Importação e Exportação 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 MEDTEC SUPPLIES, INDUSTRIA, IMPORTACAO, EXPORTACAO, DISTRIBUICAO E COMERCIO LTDA, E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
81042210003
Registration Details
ANVISA Registration Number: 81042210003
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Kit Renal Amplatz
Risk Class II

Registration Details

81042210003

25351699371201813

17035479000102

Company Information

GTA SRL
Italy
PT: ITÁLIA

Dates and Status

Dec 03, 2018

VIGENTE

09/18/2025 19:00:01