ANCHOR - ANVISA Registration 80005430471

Access comprehensive regulatory information for ANCHOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80005430471 and manufactured by manufacturer not specified. The registration is held by STRYKER DO BRASIL LTDA with validity until Jul 10, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including STRYKER ENDOSCOPY, SMITH & NEPHEW INC., ENDOSCOPY DIVISION (ANDOVER), 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.