Guide Wire - ANVISA Registration 10275160027
Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10275160027 and manufactured by SAFEWIRE LLC. The registration is held by SUPORTE HOSPITALAR LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.

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Registration Details
10275160027
25351701954201291
73857393000128
Company Information
Dates and Status
Apr 29, 2013
VIGENTE
09/18/2025 19:00:01
Guide Wire
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STARTER
LAKE REGION MEDICAL
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Not specified
80005430318
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Guide Wire
Synchro 2 - Fio Guia
STRYKER NEUROVASCULAR
80005430318
Aug 11, 2014
E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME• Brazil
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Fio Guia
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81231550085
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Fio Guia
Fio guia para Angioplastia
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD
81231550085
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Fio Guia
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LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD
80102519363
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Fio Guia
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BROSMED MEDICAL CO., LTD
81778819078
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Fio Guia
SUPERGET FIO GUIA SUPER RĂŤGIDO
NEUROINTER MEDICAL CO., LTDA
82531179008
Aug 11, 2025