Instrument for Lens Placement - ANVISA Registration 80420200077

Access comprehensive regulatory information for Instrument for Lens Placement in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80420200077 and manufactured by EYEOL UK LTD. The registration is held by VISION LINE IMPORTAÇÃO E COMÉRCIO DE MATERIAIS E EQUIPAMENTOS MÉDICOS LTDA-ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including RET, INC., BIOTECH VISION CARE PVT. LTD, 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.