Instrument for glucose - Point of Care Testing (professional) - ANVISA Registration 80954880191

Access comprehensive regulatory information for Instrument for glucose - Point of Care Testing (professional) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80954880191 and manufactured by SD BIOSENSOR,INC.. The registration is held by Eco Diagnostica Ltda with validity until Nov 07, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including TAIDOC TECHNOLOGY CORPORATION, DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME, and 4 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.