Guide - ANVISA Registration 10330520068
Access comprehensive regulatory information for Guide in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10330520068 and manufactured by Foremount Enterprise CO., Ltd. The registration is held by OXIGEL MATERIAIS HOSPITALARES, IND.E COMERCIO 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 DPS INDUSTRIA, DISTRIBUICAO, COMERCIO, IMPORTACAO E EXPORTACAO LTDA, CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA., 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
10330520068
25351429512201493
49353956000166
Company Information
Dates and Status
Aug 11, 2014
VIGENTE
09/18/2025 19:00:01
Guide Wire
SONDA GUIA
COOK INCORPORATED
10330710006
Jan 10, 2000
Guide Wire
FIO GUIA
KOBI MEDIZINTECHNIK GMBH
10368410002
May 28, 1999
Guide Wire
FIO GUIA
ISTEM MEDIKAL TIBBI CIHAZ VE SAN. TIC. LTD.STI
80591500005
Jun 19, 2017
Guide Wire
FIO GUIA
ISTEM MEDIKAL TIBBI CIHAZ VE SAN. TIC. LTD.STI
80591500010
Jun 19, 2017
Guide Wire
fio guia
BROSMED MEDICAL CO., LTD
10210419001
Jun 17, 2021
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ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD.• China
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