ANVISA registration

Flexor Tendon Sheath Retractor and Suture Retriever/Sheath Dilator Kit

Registration 81208020001. Kit Instrumental

Registration details

Registration number81208020001
Application number25351591419201604
Technical nameKit Instrumental
Risk classII
Published on30/01/2017
ValidityIndefinite validity

Registration holder

Legal nameTRIMED BRASIL IMPORTAÇÃO E DISTRIBUIÇÃO LTDA
CNPJ05.334.383/0001-58

Manufacturer

  • TOBY ORTHOPEDICS INC. ESTADOS UNIDOS DA AMÉRICA

Other registrations held by TRIMED BRASIL IMPORTAÇÃO E DISTRIBUIÇÃO LTDAview all

PLACAS ESPECIAIS MMF TRIMED

81208020002

SISTEMA DE PLACAS DE PUNHO TRIMED

81208020003

PARAFUSO MMF TRIMED

81208020004

PARAFUSO CANULADO MMF TRIMED

81208020005

PARAFUSO CANULADO PGF TRIMED

81208020006

PARAFUSO PGF TRIMED

81208020007

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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