BEUDAMED
    45 results · 23ms · 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.
    Filters Regulation: Us FDA ×

    KIRSCHNER AND GUIDE WIRES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROMANELLI DEBAKEY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896090996·ROMANELLI DEBAKEY CLAMP

    ROMANELLI DEBAKEY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921007360·ROMANELLI DEBAKEY CLAMP

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 18, 2015

    STAIR SYSTEMS PACS & DICOM VIEWER

    FDA 510(k)
    FDA Class 2 ·Radiology

    LA JOIE

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 3, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 4, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·October 8, 2015

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITI·May 8, 2013

    TROCHANTERIC FIXATION NAIL SCREW INSERTER/EXTRACTOR

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HSB·September 19, 2014

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·May 18, 2011

    GYNECARE TVT-ABBREVO MINI LCM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·November 30, 2021

    VA LOCKSCR Ø2.4 SELF-TAP L24 TAN

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013

    VA LOCKSCR Ø2.4 SELF-TAP L24 TAN

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013

    2.4MM TI VA LOCKING SCREW STARDRIVE 22MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013

    2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 11MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·December 22, 2014

    BD VACUTAINER® CAT (CLOT ACTIVATOR TUBE) PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 3, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·October 7, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·October 3, 2014