Cystoscope - ANVISA Registration 81769779002
Access comprehensive regulatory information for Cystoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81769779002 and manufactured by SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD.. The registration is held by ENDO MED PRODUTOS MEDICOS 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 SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD., TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH, 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.
Device Details
Registration Details
81769779002
25351263774202395
29397137000103
Company Information
Dates and Status
May 22, 2023
VIGENTE
09/18/2025 19:00:01
Cistoscópio
Endoscopio para Cistoscopia Mistra
SCHOLLY FIBEROPTIC GMBH
10302869026
Aug 25, 2025
Cistoscópio
Endoscópio Rígido para Uretro-cistoscopia/Urologia Mistra
TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH
10302869021
Aug 04, 2025
Cistoscópio
Cistoscópio de Vídeo Flexível
SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD.
80686369116
Apr 14, 2025

