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

Filters - ANVISA Registration 80136999101

Access comprehensive regulatory information for Filters in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80136999101 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 companies making the same product including INTERSURGICAL LTD., MERCK MILLIPORE LTD, 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
80136999101
Registration Details
ANVISA Registration Number: 80136999101
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

OMNISet® TPE - Kit para tratamento de plasma
Risk Class II

Registration Details

80136999101

25351459750202411

31673254000102

Company Information

B. BRAUN AVITUM AG
Germany
PT: ALEMANHA

Dates and Status

Jan 06, 2025

VIGENTE

09/18/2025 19:00:01