Instrument for glucose - Point of Care Testing (professional) - ANVISA Registration 80954880180

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 80954880180 and manufactured by TAIDOC TECHNOLOGY CORPORATION. The registration is held by Eco Diagnostica Ltda with validity until Nov 29, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including SD BIOSENSOR,INC., 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.