International safety notice

URGENT MEDICAL DEVICE CORRECTION for ARIA® for Radiation Oncology, ARIA® Oncology Information System for Radiation Oncology, Varian

Germany / BfArM · DEU · Nov 3, 2015

Key facts

Title URGENT MEDICAL DEVICE CORRECTION for ARIA® for Radiation Oncology, ARIA® Oncology Information System for Radiation Oncology, Varian
Regulator Germany / BfArM
Country DEU
Brand Radiation Oncology, Varian
Manufacturer URGENT MEDICAL DEVICE CORRECTION for ARIA® for Radiation Oncology, ARIA® Oncology Information System for Radiation Oncology, Varian
Models 2015-09-29, 1.888.4265, CP-21350, L5463
Date Nov 3, 2015
Regulator page bfarm.de

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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