Fistula Needle - ANVISA Registration 80136990877

Access comprehensive regulatory information for Fistula Needle in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80136990877 and manufactured by B. BRAUN AVITUM AG. The registration is held by LABORATORIOS B. BRAUN S/A 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 BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD, BIOTEQUE CORPORATION, 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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80136990877
Registration Details
ANVISA Registration Number: 80136990877
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Agulhas de FĂ­stula Diacan Pro
Risk Class II

Registration Details

80136990877

25351384664201707

31673254000102

Company Information

B. BRAUN AVITUM AG
Germany
PT: ALEMANHA

Dates and Status

Aug 14, 2017

VIGENTE

09/18/2025 19:00:01