Buffer - ANVISA Registration 80285220014

Access comprehensive regulatory information for Buffer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80285220014 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.