ANCHOR - ANVISA Registration 10306840205

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 10306840205 and manufactured by manufacturer not specified. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA with validity until Jul 08, 2034.

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.