ANVISA registration

TRANSFER DEVICE

Registration 80145110205. Dispositivos

Registration details

Registration number80145110205
Application number25351477901200801
Technical nameDispositivos
Risk classII
Published on15/09/2008
ValidityIndefinite validity

Registration holder

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

Manufacturing sites

  • FABRICADO POR CLINICO MEDICAL PRODUCTION GMBH - ALEMANHA PARA FRESENIUS KABI AG ALEMANHA
  • FABRICADO POR: CLINICO MEDICAL SP.Z. O O BLONIE K/WROCLAWIA - POLÔNIA PARA FRESENIUS KABI AG ALEMANHA
  • FABRICADO POR: CLINICO NANCHANG LTD. CO. - REPÚBLICA POPULAR DA CHINA PARA FRESENIUS KABI AG ALEMANHA
  • FABRICADO POR: FRESENIUS KABI DEUTSCHLAND GMBH - ALEMANHA PARA 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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