International safety notice

Implantable Electrode Cable

Brazil / Anvisa · BRA · Jan 6, 2015

Key facts

Title Implantable Electrode Cable
Regulator Brazil / Anvisa
Country BRA
Brand Specify electrode kit, models 39565 and 39286, registration 10339190365, risk class IV, various lots (SEE ANNEX).
Manufacturer DETENTOR DO REGISTRO MEDTRONIC COMERCIAL LTDA ENDEREÇO AV JORNALISTA ROBERTO MARINHO 85 9º ANDAR PARTE E 10º ANDAR PARTECEP 04675010 FABRICANTE VÁRIOS VER ANEXO
Models 39565, 39286, 10339190365
Date Jan 6, 2015
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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