ANCHOR - ANVISA Registration 80804050202

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 80804050202 and manufactured by SMITH & NEPHEW INC., ENDOSCOPY DIVISION (ANDOVER). The registration is held by Smith & Nephew Comércio de Produtos Médicos Ltda. with validity until Jul 04, 2026.

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 STRYKER ENDOSCOPY, ARTHREX, INC., 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.