Camera - ANVISA Registration 80133510003

Access comprehensive regulatory information for Camera in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80133510003 and manufactured by SMARTPRACTICE. The registration is held by FDA ALLERGENIC FARMACEUTICA LTDA - EPP 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 FISHER & PAYKEL HEALTHCARE LIMITED, INTERSURGICAL 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.