ANVISA registration

AGULHA DE FÍSTULA DIALINE

Registration 80188510011. Agulha de Fistula

Registration details

Registration number80188510011
Application number25351335934200991
Technical nameAgulha de Fistula
Risk classII
Published on28/09/2009
ValidityIndefinite validity

Registration holder

Legal nameALLMED PRONEFRO BRASIL LTDA
CNPJ04.980.517/0001-45

Manufacturer

  • ALLMED PRONEFRO PT, S.A. PORTUGAL

Other registrations held by ALLMED PRONEFRO BRASIL LTDAview all

ISOLADOR DE PRESSÃO DIALINE

80188510002

LINHA DE SANGUE ARTERIAL PARA HEMODIALISE DIALINE

80188510013

LINHA DE SANGUE VENOSA PARA HEMODIALISE DIALINE

80188510014

CONECTORES DIALINE

80188510016

CONECTORES

80188510017

LINHA DE SANGUE ARTERIAL PARA HEMODIALISE DIALINE

80188510018

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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