Biopsy Instrument - ANVISA Registration 80686360104

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 80686360104 and manufactured by STERYLAB S.R.L.. The registration is held by MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR 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 CHAMFOND BIOTECH CO., LTD., BARD PERIPHERAL VASCULAR, INC., 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.