ANVISA registration

KIT DE CIFOPLASTIA DIRETO DUPLO KDD

Registration 10350530116. Kit Instrumental

Registration details

Registration number10350530116
Application number25351022306201437
Technical nameKit Instrumental
Risk classII
Published on12/05/2014
ValidityIndefinite validity

Registration holder

Legal nameLINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP LTDA
CNPJ01.197.835/0001-46

Manufacturer

  • SINTEA PLUSTEK S.R.L. ITÁLIA

Other registrations held by LINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP LTDAview all

CATETER PARA VENTILAÇÃO TORÁCICA TRU-CLOSE

10350530025

KIT INSULFLADOR ACCUREX

10350530061

SISTEMA DE BOLSA COLETORA URESIL

10350530065

CATETER PARA DRENAGEM URESIL

10350530074

Seringa Com Dispositivo de Segurança Com Agulha -Gmp (Global Medi Products)

10350530079

Seringas Descartável Sem Agulha

10350530081

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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