International safety notice

ProteusPLUS y ProteusONE (modelo Proteus 235

Spain / AEMPS · ESP · Feb 24, 2022

Key facts

Title ProteusPLUS y ProteusONE (modelo Proteus 235
Regulator Spain / AEMPS
Country ESP
Brand ProteusPLUS y ProteusONE (modelo Proteus 235
Manufacturer IBA (Ion Beam Applications). Bélgica
Models 77091, PAT.112, SBF.110, PAT.108, SBF.128, SBF.109, PAT.110, SAT.125, PAT109, SBF.101, PAT.003, PAT.107 and 35 more
Event type Safety Notice
Date Feb 24, 2022

At a glance

  • No Recall
  • Yes 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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