Devices - ANVISA Registration 80136990922
Access comprehensive regulatory information for Devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80136990922 and manufactured by B. BRAUN MEDICAL AG - SUIÇA. 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 APPLIED MEDICAL TECHNOLOGY, INC, ATOS MEDICAL AB, 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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Registration Details
80136990922
25351774003201861
31673254000102
Company Information
Dates and Status
May 08, 2019
VIGENTE
09/18/2025 19:00:01
Debrider
PRONTOSAN GEL
B. BRAUN MEDICAL AG - SUIÇA
80136990575
Sep 15, 2008
Debrider
PRONTOSAN GEL
Not specified
80136990575
Sep 15, 2008
Debrider
Prontosan® Wound Gel X
B. BRAUN MEDICAL AG - SUIÇA
80136990836
Aug 10, 2015
Debrider
Prontosan® Wound Gel X
Not specified
80136990836
Aug 10, 2015
Debrider
Debrisoft® Pad
LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG.
80102512177
Mar 06, 2019
APPLIED MEDICAL TECHNOLOGY, INC• United States of America
ATOS MEDICAL AB• Sweden
GABISA MEDICAL INTERNATIONAL LTDA EPP• Brazil
SEROPLAST INDÚSTRIA E COMÉRCIO DE PRODUTOS HOSPITALARES LTDA -ME• Brazil
Merit Medical System, INC.• United States of America
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