Biopsy Instrument - ANVISA Registration 81021300012

Access comprehensive regulatory information for Biopsy Instrument in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81021300012 and manufactured by Osseon Therapeutics,Inc. The registration is held by MEDSUPPLY COMÉRCIO DE 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 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.