Cystoscope - ANVISA Registration 80686369116
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 80686369116 and manufactured by SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD.. The registration is held by MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR 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 TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH, SCHOLLY FIBEROPTIC 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
80686369116
25351045053202567
09117476000181
Company Information
Dates and Status
Apr 14, 2025
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
ENDOSCÓPIO FLEXÍVEL SeeScope
SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD.
81769779002
May 22, 2023

