EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS - ANVISA Registration 10230730110

Access comprehensive regulatory information for EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10230730110 and manufactured by HELENA LABORATORIES, INC.. The registration is held by NL COMÉRCIO EXTERIOR 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 WALLAC OY, ABBOTT MOLECULAR 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.