International safety notice

Urgent Field Safety Notice for Proteus 235/ProteusPLUS by IBA (Ion Beam Applications)

Germany / BfArM · DEU · Feb 2, 2018

Key facts

Title Urgent Field Safety Notice for Proteus 235/ProteusPLUS by IBA (Ion Beam Applications)
Regulator Germany / BfArM
Country DEU
Brand Proteus 235/ProteusPLUS
Manufacturer IBA (Ion Beam Applications)
Models PR-78667, OCCURS2, PAT-112, PAT.108, ACQI0N$, PTS-8.XX, PAT.107, PTS-7.XX, PAT-113
Date Feb 2, 2018
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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