Buffer - ANVISA Registration 80285220009

Access comprehensive regulatory information for Buffer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80285220009 and manufactured by BESS MEDIZINTECHNIK GmbH. The registration is held by LANG E FILHOS MATERIAL HOSPITALAR LTDA ME 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 MEDTRONIC XOMED, INC., SPIGGLE & THEIS MEDIZINTECHNIK GMBH, 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.