BEUDAMED
    7 results · 18ms · 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 ×

    TITAN GEL IFE TRIVALENT ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Immunology

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011891188000·1 case discovery® Ricketts Universal 18 Bracke...

    ASAHI ZENYTEEX GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ASHK100G

    FDA 510(k)
    FDA Class 2 ·Radiology

    CROSS PLATE MTP, LEFT ANCHORAGE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·June 24, 2014

    ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NTE·November 4, 2010

    PCA3 MEDNET WIRELESS

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code MEA·December 21, 2012