BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    THE COBALT SCALPEL

    FDA 510(k)
    FDA Class 2 ·Radiology

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295234456·P.F.C. SIGMA DISTAL AUGMENT COMBO SIZE 4 16mm R...

    PFC*SIGMA DI AUG16MMCO,SZ4RGHT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JWH·March 24, 2021

    Suction Pump (SU-90)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GALILEOS

    FDA 510(k)
    FDA Class 2 ·Dental

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 27, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 30, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 12, 2011