International safety notice

Equipment

Brazil / Anvisa · BRA · Feb 17, 2014

Key facts

Title Equipment
Regulator Brazil / Anvisa
Country BRA
Brand LA VITA BURETTE EQUIPMENT, Registration no. 80288099006, lot: KLB5-120710A, Fab.
Manufacturer DETENTOR DO REGISTRO NO BRASIL TKL IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS E HOSPITALARES LTDA CNPJ 07415627000152 ENDEREÇO RUA ENGENHEIRO JULIO CESAR DE SOUZA ARAUJO N 220 CIC CURITIBAPR
Models KLB5-120710A, 80288099006
Date Feb 17, 2014
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

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