ANVISA registration

Produto para Cateterização Venosa Central de Lúmen Duplo

Registration 80312270061. Cateteres

Registration details

Registration number80312270061
Application number25351041184202575
Technical nameCateteres
Risk classIV
Published on01/09/2025
ValidityValid until 31/12/2028

Registration holder

Legal nameTELEFLEX MEDICAL BRASIL LTDA
CNPJ06.089.071/0001-99

Manufacturer

  • ARROW INTERNATIONAL LLC (SUBSIDIARY OF TELEFLEX INCORPORATED) ESTADOS UNIDOS DA AMÉRICA

Other registrations held by TELEFLEX MEDICAL BRASIL LTDAview all

PLEUR-EVAC

80312270008

TROCAR LAPAROSCÓPIO WECK VISTA PORT SMOOTH

80312270011

TROCAR LAPAROSCÓPICO WECK VISTA CONE OPEN ACESS PORT

80312270012

TROCAR LAPAROSCÓPIO WECK VISTA PORT RIDGE

80312270013

TROCAR LAPAROSCÓPICO WECK VISTA BALLON OPEN ACESS PORT

80312270014

ENDO FACIAL CLOSURE SYSTEM

80312270015

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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