GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR - ANVISA Registration 82214249015
Access comprehensive regulatory information for GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82214249015 and manufactured by ALTON (SHANGHAI) MEDICAL INSTRUMENTS CO., LTD. The registration is held by LYNX PRODUTOS MEDICOS LTDA. with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION, BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED, 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.
Device Details
Registration Details
82214249015
25351123694202560
08587310000166
Company Information
Dates and Status
Jul 28, 2025
VIGENTE
09/18/2025 19:00:01
FIO GUIA DE USO GERAL, NÃO VASCULAR
FIO GUIA HIDROFÍLICO UROPRO TAIMIN
HUNAN VMT TECHNOLOGY CO., LTD.
80082919068
Aug 25, 2025
FIO GUIA DE USO GERAL, NÃO VASCULAR
FIO GUIA ZEBRA UROPRO TAIMIN
HUNAN VMT TECHNOLOGY CO., LTD.
80082919070
Aug 25, 2025
FIO GUIA DE USO GERAL, NÃO VASCULAR
FIO GUIA ZEBRA COM PONTA HIDROFÍLICA UROPRO TAIMIN
HUNAN VMT TECHNOLOGY CO., LTD.
80082919073
Aug 25, 2025
FIO GUIA DE USO GERAL, NÃO VASCULAR
FIO GUIA NÃO-VASCULAR HIDROFÍLICO MEDICONE
MEDICONE PROJETOS E SOLUÇÕES PARA A INDÚSTRIA E A SAÚDE LTDA
80020559012
Jul 21, 2025
FIO GUIA DE USO GERAL, NÃO VASCULAR
Fio Guia para Procedimentos Endoscópicos
G-FLEX EUROPE SPRL (NIVELLES)
10334789014
Jun 02, 2025

