BEUDAMED
    11 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 ×

    Foundation Interbody Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AGXO

    FDA UDI
    Oticon A/S·05707131280978·H160V2, BTE 13 WL 100 TC AGXO

    BD BBL¿ THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITAMIN K1, AND HEMIN

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JSG·August 27, 2019

    BD BBL¿ THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITAMIN K1, AND HEMIN

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code JSG·September 24, 2019

    IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SYNTHETIC SEEDING SPACER MODEL SS9 X 50-50, SS9 X 55-50, SS9 X 55-150, SS9 X 1CM-30

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD BBL¿ THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITAMIN K1, AND HEMIN

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JSG·November 22, 2019

    X-SUIT NIR COVERED BILIARY METALLIC STENT

    FDA Adverse Event
    Malfunction ·MEDINOL LTD.·Product code FGE·December 27, 2017

    ALTRUA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 8, 2014

    COULTER® AC *T DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 6, 2013

    AUGMENTED INSERT

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 29, 2011