ANVISA registration

Fio Guia Hidrofílico ACE

Registration 81403789002. Fio Guia

Registration details

Registration number81403789002
Application number25351178479202334
Technical nameFio Guia
Risk classII
Published on03/04/2023
ValidityIndefinite validity

Registration holder

Legal nameARQUIMED DISTRIBUIDORA E REPRESENTACAO DE PRODUTOS MEDICOS LTDA
CNPJ23.241.814/0001-13

Manufacturer

  • ACE MEDICAL DEVICES PVT. LTD. (EAST AVENUE) ÍNDIA

Other registrations held by ARQUIMED DISTRIBUIDORA E REPRESENTACAO DE PRODUTOS MEDICOS LTDAview all

Família Teste de anticorpo SARS-CoV-2 (imunocromatografia - ouro coloidal)

81403780001

Kit de Teste Rápido com Antígeno de SARS-CoV-2

81403780002

Kit de Teste Rápido para Autoteste de Deteção de Antigénio do vírus SARS-CoV-2

81403780003

Família Alça de ressecção e vaporização eletrocirúrgica bipolar ACE

81403780004

Família de Agulhas EBUS Ecoendoscopia

81403789001

Bainha de Acesso Ureteral Hidrofílico ACE

81403789003

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

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