International safety notice

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Brazil / Anvisa · BRA · Jun 16, 2012

Key facts

Title .
Regulator Brazil / Anvisa
Country BRA
Brand ALLURA XPER ANGIOGRAPHY EQUIPMENT.
Manufacturer DETENTOR DE REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178
Models 10216710206, 10216710153
Date Jun 16, 2012
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 100–999 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