Guide Wire - ANVISA Registration 81231550085
Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81231550085 and manufactured by manufacturer not specified. The registration is held by Total Life comercio de produtos Medico-Hospitalar LTDA-EPP with validity until Sep 15, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, SP MEDICAL A/S, 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
81231550085
25351377601202434
21310535000139
Company Information
Dates and Status
Sep 15, 2025
15/09/2035
09/18/2025 19:00:01
E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME• Brazil
SP MEDICAL A/S• Denmark
MEDTEC SUPPLIES, INDUSTRIA, IMPORTACAO, EXPORTACAO, DISTRIBUICAO E COMERCIO LTDA• Brazil
SHUNMEI MEDICAL Co., Ltd• China
SHENZHEN MICROAPPROACH MEDICAL TECHNOLOGY CO., LTD.• China
Fio Guia
Fio-guia Hidrofílico Periférico Wriggle
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD
80102519363
Aug 25, 2025
Fio Guia
Fio-guia Khons
BROSMED MEDICAL CO., LTD
81778819078
Aug 11, 2025
Fio Guia
SUPERGET FIO GUIA SUPER RÍGIDO
NEUROINTER MEDICAL CO., LTDA
82531179008
Aug 11, 2025
Fio Guia
HYDROFIBER - FIO GUIA HIDROFÍLICO
ITS DO BRASIL INDUSTRIA E COMÉRCIO DE PRODUTOS MÉDICOS LTDA
82130519029
Aug 04, 2025
Fio Guia
FIO GUIA HIDROFÍLICO
MANISH MEDI INNOVATION
83032659011
Aug 04, 2025

