Capsule Endoscopy System - ANVISA Registration 10306849029

Access comprehensive regulatory information for Capsule Endoscopy System in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10306849029 and manufactured by CAPSOVISION, INC.. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including GIVEN IMAGING, INC., INTROMEDIC CO., LTD, 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.