ANVISA registration

Kit Dilatador Amplatz

Registration 80733590011. Kit Instrumental

Registration details

Registration number80733590011
Application number25351109955201991
Technical nameKit Instrumental
Risk classII
Published on30/09/2019
ValidityIndefinite validity

Registration holder

Legal nameANSER-BR COMERCIO DE PRODUTOS PARA SAUDE LTDA
CNPJ11.825.879/0001-27

Manufacturer

  • DLR MEDIKAL SAN. VE DIS. TIC. LTD. STI TURQUIA

Other registrations held by ANSER-BR COMERCIO DE PRODUTOS PARA SAUDE LTDAview all

Endoscópio

80733590001

Cateter Ureteral Duplo J

80733590002

Cateter Ureteral

80733590003

Fio Guia Hidrofílico

80733590004

Trocarte Endoscópico

80733590005

Bainha de Acesso Ureteral

80733590006

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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