BEUDAMED
    10 results · 34ms · 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.

    BARTELS TOXOPLASMA IGM EIA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VELASHAPE

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

    STRYKER NAVIGATION SYSTEM-KNEE MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

    SUPRIS RETROPUBIC KIT

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code OTN·May 22, 2018

    SUPRIS RETROPUBIC KIT

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code OTN·May 22, 2018

    PACS IW

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code LLZ·November 19, 2010

    SECURE 3 MED/SURG ZOOM BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 18, 2013

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·July 9, 2014