BEUDAMED
    7 results · 19ms · 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.

    MammoSTAR Biopsy Site Identifier

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

    Sonic

    FDA UDI
    Sbo Hearing A/S·05714464089000·SONIC ENCHANT SE 10 ITE FS

    HEMOGLIDE SERIES AND HEMOGLIDE STAR SERIES XK LONG-TERM HEMODIALYSIS CATHETERS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Clean & More

    FDA 510(k)
    FDA Class 2 ·Dental

    ETHILON NYLON SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAR·December 3, 2008

    ALARIS SYRINGE MODULE SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·August 31, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 29, 2013