Ureterorenoscope - ANVISA Registration 80082919052
Access comprehensive regulatory information for Ureterorenoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80082919052 and manufactured by MDKMED MEDICAL TECHNOLOGY CO., LTD.. The registration is held by CIENLABOR INDUSTRIA E COMERCIO LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including CONFIANCE MEDICAL PRODUTOS MÉDICOS S.A., DEUTSCHLINE MEDIZINPRODUKTE GMBH, and 4 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
80082919052
25351103357202556
02814280000105
Company Information
Dates and Status
Jul 21, 2025
VIGENTE
09/18/2025 19:00:01
Ureterorrenoscópio
Endoscopio para Ureterorrenoscopia Mistra
SCHOLLY FIBEROPTIC GMBH
10302869027
Aug 25, 2025
Ureterorrenoscópio
PROBE DEUTSCHLINE
DEUTSCHLINE MEDIZINPRODUKTE GMBH
81901539030
Jun 16, 2025
Ureterorrenoscópio
Endoscópio Rígido
CONFIANCE MEDICAL PRODUTOS MÉDICOS S.A.
80337659006
Apr 08, 2024
Ureterorrenoscópio
Flexível Digital Reutilizável
BONREE MEDICAL CO. LTD.
81655779001
Dec 03, 2018

