Laser Device For Ophthalmic Diagnosis - ANVISA Registration 80418650002

Access comprehensive regulatory information for Laser Device For Ophthalmic Diagnosis in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80418650002 and manufactured by HEIDELBERG ENGINEERING GMBH. The registration is held by ZETA VISION COMERCIO DE PRODUTOS OTICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including HAAG-STREIT AG, ALCON LABORATORIES, INC, and 3 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.