32 results
·
42ms
·
Sources: EU EUDAMED, US FDA
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222098546312017201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022209854631317201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222098546338117201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022209854631217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222098546312717201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022209854633217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222098546338217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222098546315917201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022209854632517201·BTE-TRT
Set, Administration, Intravascular
FDA classification
FDA Class 2
·Set, Administration, Intravascular
Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
FDA classification
FDA Class 2
·Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)