SQUAMOUS CELL CARCINOMA ANTIGEN - ANVISA Registration 80254180373

Access comprehensive regulatory information for SQUAMOUS CELL CARCINOMA ANTIGEN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180373 and manufactured by B-R-A-H-M-S GMBH. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Sep 08, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, ABBOTT GMBH, 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.