Buffer - ANVISA Registration 80709150007

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 80709150007 and manufactured by AD MED&#304.KAL VE SA&#286.LIK ÜR. SAN. &#304.C VE DI&#350. T&#304.C LTD. ST&#304... The registration is held by SURGICAL GROUP IMPORTACAO E EXPORTACAO LTDA 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.