URINARY STENT - ANVISA Registration 80073110104
Access comprehensive regulatory information for URINARY STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80073110104 and manufactured by UROTECH GmbH. The registration is held by MEDI-GLOBE BRASIL LTDA with validity until Apr 01, 2029.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED, BOSTON SCIENTIFIC CORPORATION, and 5 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.
Related Devices (2)
Registration Details
80073110104
25351220058201712
04242860000192
Company Information
Dates and Status
Apr 01, 2019
01/04/2029
09/18/2025 19:00:01
STENT URINÁRIO
KIT CATETER DUPLO J COM FIO GUIA TEFLONADO UROPRO TAIMIN
HUNAN VMT TECHNOLOGY CO., LTD.
80082919064
Aug 25, 2025
STENT URINÁRIO
KIT CATETER DUPLO J COM FIO GUIA HIDROFÍLICO UROPRO TAIMIN
HUNAN VMT TECHNOLOGY CO., LTD.
80082919065
Aug 25, 2025
STENT URINÁRIO
CATETER DUPLO J UROPRO TAIMIN
HUNAN VMT TECHNOLOGY CO., LTD.
80082919069
Aug 25, 2025
STENT URINÁRIO
CATETER DUPLO J HIDROFÍLICO UROPRO TAIMIN
HUNAN VMT TECHNOLOGY CO., LTD.
80082919074
Aug 25, 2025
STENT URINÁRIO
B-INDOVASIVE-BIOFLEX
Not specified
80686360433
Aug 18, 2025

