Sinoscope - ANVISA Registration 82747889012

Access comprehensive regulatory information for Sinoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82747889012 and manufactured by ANQING CHANGFAN MEDICAL INSTRUMENT CO., LTD. The registration is held by ONE SURG COMERCIAL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including SCHOLLY FIBEROPTIC GMBH, and 1 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.