Instrument for glucose - Point of Care Testing (professional) - ANVISA Registration 80638729002

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 80638729002 and manufactured by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Feb 15, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including SD BIOSENSOR,INC., TAIDOC TECHNOLOGY CORPORATION, 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.