International safety notice

Technical name: STENT FOR PERIPHERAL ARTERIES

Brazil / Anvisa · BRA · Dec 13, 2016

Key facts

Title Technical name: STENT FOR PERIPHERAL ARTERIES
Regulator Brazil / Anvisa
Country BRA
Brand Trade name: NITINOL CORDIS STENTS Technical name: STENT FOR PERIPHERAL ARTERIES ANVISA registration number: 80145901077 Risk class: IV Affected model: PC0540XCE;
Manufacturer NOTIFICAÇÃO FEITA PELA EMPRESA EM ATENDIMENTO À RDC 232012 QUE DISPÕE SOBRE A OBRIGATORIEDADE DE EXECUÇÃO E NOTIFICAÇÃO DE AÇÃO DE CAMPO POR PARTE DO DETENTOR DO REGISTRO DO PRODUTO PARA A SAÚDE EMPRESA DETENTORA DO REGISTRO JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA FABRICANTE JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA RUA GERIVATIBA 207 SÃO PAULO
Models PC0720XCE, PC0620XCE, PC0730XCE, PC0920XCE, 80145901077, PC0830XCE, PC0930XCE, PC0540XCE, PC1040XCE, PC1020XCE, PC0630XCE, PC0940XCE and 3 more
Date Dec 13, 2016
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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

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