Biopsy Instrument - ANVISA Registration 81769770015

Access comprehensive regulatory information for Biopsy Instrument in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81769770015 and manufactured by TONTARRA MEDIZINTECHNIK GMBH. The registration is held by ENDO MED PRODUTOS MEDICOS 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 STERYLAB S.R.L., CHAMFOND BIOTECH CO., 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.