Vitrectomy Unit - ANVISA Registration 80136060388

Access comprehensive regulatory information for Vitrectomy Unit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80136060388 and manufactured by BAUSCH & LOMB INCORPORATED. The registration is held by BL INDÚSTRIA OTICA LTDA with validity until Oct 07, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 1 companies making the same product including BAUSCH & LOMB INCORPORATED, and 2 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.