SELF-TEST INSTRUMENT FOR GLUCOSE, URIC ACID AND KETONE BODIES - ANVISA Registration 81692610290

Access comprehensive regulatory information for SELF-TEST INSTRUMENT FOR GLUCOSE, URIC ACID AND KETONE BODIES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81692610290 and manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD.. The registration is held by VYTTRA DIAGNOSTICOS S.A. with validity until Jun 03, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.