ANVISA registration

SONDA DE FIBRA ÓPTICA PARA HOLMIUM LASER MAXIFLEX

Registration 80518270004. fibra optica

Registration details

Registration number80518270004
Application number25351334259201089
Technical namefibra optica
Risk classIII
Published on16/04/2012
ValidityValid until 16/04/2027

Registration holder

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

Manufacturer

  • MAXIFLEX, LLC/TECHNOLOGY DELIVERY SYSTEMS, INC ESTADOS UNIDOS DA AMÉRICA

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

DISPOSITIVO DE INFLAÇÃO ID

80518270003

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

KIT Dilatador Renal ALLWIN

80518270009

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.

Next step

Medical device registration with ANVISA

HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.

Speak to a specialist