ANVISA registration

Extensor para Equipo Enteral Applix

Registration 80145119011. Extensor

Registration details

Registration number80145119011
Application number25351696249201487
Technical nameExtensor
Risk classII
Published on22/12/2014
ValidityIndefinite validity

Registration holder

Legal nameFRESENIUS KABI BRASIL LTDA
CNPJ49.324.221/0001-04

Manufacturer

  • FRESENIUS KABI AG ALEMANHA

Other registrations held by FRESENIUS KABI BRASIL LTDAview all

FREKA-SONDA ENTERAL

10004100022

SOLUCAO EURO-COLLINS - Para Perfusao de rins em transplante

10004100066

FREKA SONDA ENTERAL CH 15

10004100145

FREKA PAED CH 6,5

10004100147

EQUIPO PARA SANGUE E HEMODERIVADOS

80145110160

EQUIPO PARA INFUSAO DE MEDICAMENTOS FOTOSSENSIVEIS OP MS PARA BOMBA DE INFUSAO

80145110161

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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