International safety notice

Safety Notice for VITROS® 5600 Integrated System and VITROS® 3600 Immunodiagnostic System, Ortho-Clinical Diagnostics

Germany / BfArM · DEU · Nov 24, 2010

Key facts

Title Safety Notice for VITROS® 5600 Integrated System and VITROS® 3600 Immunodiagnostic System, Ortho-Clinical Diagnostics
Regulator Germany / BfArM
Country DEU
Brand VITROS® 5600 Integrated System and VITROS® 3600 Immunodiagnostic System, Ortho-Clinical Diagnostics
Manufacturer Safety Notice for VITROS® 5600 Integrated System and VITROS® 3600 Immunodiagnostic System, Ortho-Clinical Diagnostics
Models PVD-019, CL10-231A_EU, CL10-231A
Date Nov 24, 2010
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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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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