International safety notice

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Brazil / Anvisa · BRA · Jun 14, 2012

Key facts

Title .
Regulator Brazil / Anvisa
Country BRA
Brand ARTERIAL SARNS CANNULA (Anvisa Registration No. 80012280001).
Manufacturer FABRICANTE TERUMO CARDIOVASCULAR SYSTEMS EUA DETENTOR DE REGISTRO TERUMO MEDICAL DO BRASIL LTDA CNPJ 03129105000133 END RUA GOMES DE CARVALHO 1507 CJ 151152 CEP04547005 VILA OLÍMPIA SÃO PAULOSP TEL 11 35943845 FAX 11 35943845
Models 0571580, 0570456, 80012280001, 0644444, 0640518, 0646144, 0650900, 13010, 13020, 0666574, 13030, 0574279 and 8 more
Date Jun 14, 2012
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 Matching catalog numbers in FDA data

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

Browse all International device safety notices