Guide Wire - ANVISA Registration 82003529002
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 82003529002 and manufactured by ZHEJIANG SOUDON MEDICAL TECHNOLOGY CO.,LTD. The registration is held by MANANCIAL MEDICAL 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
82003529002
25351044917202523
24603766000129
Company Information
Dates and Status
Apr 14, 2025
VIGENTE
09/18/2025 19:00:01
Guide Wire
FIO GUIA DESCARTAVEL
TERUMO CORPORATION
80124630102
Jan 22, 2007
Guide Wire
FIO GUIA DESCARTÁVEL
PRINCE MEDICAL
10368419005
May 31, 2011
Guide Wire
Fio-guia graduado descartável
ZHEJIANG YIGAO MEDICAL TECHNOLOGY CO., LTD.
82195309022
Nov 04, 2024
Guide Wire
Fio Guia Hidrofilico
Xiamen New Concept Medical Technology Co.ltd
80160400110
Oct 10, 2016
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Fio Guia hidrofilico
ALLIGATOR MEDICAL SOCIEDAD ANONIMA
80222919001
Jan 13, 2022
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
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Not specified
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SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD
81231550085
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80102519363
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BROSMED MEDICAL CO., LTD
81778819078
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SUPERGET FIO GUIA SUPER RÍGIDO
NEUROINTER MEDICAL CO., LTDA
82531179008
Aug 11, 2025