ANVISA registration

STENT URETERAL COM FIO GUIA TEFLONADO ALLWIN

Registration 80518270020. Stent Ureteral

Registration details

Registration number80518270020
Application number25351198166201445
Technical nameStent Ureteral
Risk classII
Published on21/07/2014
ValidityIndefinite validity

Registration holder

Legal nameEIC BRASIL EXPORTADORA DE PRODUTOS INDUSTRIALIZADOS LTDA
CNPJ09.209.604/0001-17

Manufacturing sites

  • ALLWIN MEDICAL DEVICES ESTADOS UNIDOS DA AMÉRICA
  • ALLWIN MEDICAL DEVICES ÍNDIA

Other registrations held by EIC BRASIL EXPORTADORA DE PRODUTOS INDUSTRIALIZADOS LTDAview all

DISPOSITIVO DE INFLAÇÃO ID

80518270003

SONDA DE FIBRA ÓPTICA PARA HOLMIUM LASER MAXIFLEX

80518270004

Sonda de acesso ureteral U-Flex ALLWIN

80518270005

CATETER EXTRATOR DE CÁLCULO U-PERC NITINOL ALLWIN

80518270006

Dilatador Ureteral ALLWIN

80518270007

Fio Guia Hidrofílico ALLWIN

80518270008

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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