ANVISA registration

MEIA ANTI-EMBOLISMO T.E.D. KENDALL

Registration 81356112302. Meia Anti-Embolismo

Registration details

Registration number81356112302
Application number25351552101201840
Technical nameMeia Anti-Embolismo
Risk classI
Published on03/09/2018
ValidityIndefinite validity

Registration holder

Legal nameCARDINAL HEALTH DO BRASIL LTDA.
CNPJ19.585.158/0001-07

Manufacturing sites

  • COVIDIEN llC ESTADOS UNIDOS DA AMÉRICA
  • COVIDIEN, anteriormente registrada como Kendall, a division of Tyco Healthcare Group LP ESTADOS UNIDOS DA AMÉRICA
  • Covidien UK Ltd., anteriormente registrada como Tyco Healthcare UK Manufacturing Ltd. REINO UNIDO
  • KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP ESTADOS UNIDOS DA AMÉRICA

Other registrations held by CARDINAL HEALTH DO BRASIL LTDA.view all

Cateter de Reentrada OUTBACK Elite

81356110000

CATETER FRONTRUNNER XP CTO

81356110001

Cateter de suporte Cordis ELITECROSS

81356112176

CATETER DE REINTRODUCAO OUTBACK LTD

81356112274

AGULHA ANGIOGRAFICA

81356112275

SABER PTA Dilatation Catheter

81356112290

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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