BEUDAMED
    8 results · 20ms · 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 ×

    SYNTHES (USA) (SYNTHES) SINGLE VECTOR DISTRACTOR WITH DETACHABLE FEET

    FDA 510(k)
    FDA Class 2 ·Dental

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981075·anteriors; shade A3; mould UL2

    PAINSHIELD MD

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PureSet Tray

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·March 4, 1998

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·February 19, 2013

    ENPULSE

    FDA Adverse Event
    Death ·MEDTRONIC S.A.·Product code DXY·February 8, 2011

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 24, 2014