BEUDAMED
    1,178 results · 39ms · 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 ×

    Hood, Small Multi-Use

    FDA UDI
    ACCUTRON, INC.·00813830021561·

    RE-BAG MULTI-USE POUCH, LARGE & SMALL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NIBP Cuffs

    FDA UDI
    Philips Medical Systems Hsg·20884838037711·Multi Care Cuff, Small Adult (light blue). Circ...

    40948 Small Multi-Angle Wedge

    FDA UDI
    XODUS MEDICAL, INC.·00787551039580·40948 Small Multi-Angle Wedge

    Small Multi Use Non Scavenger Cir

    FDA UDI
    ACCUTRON, INC.·00813830021530·

    Scavenger W/ Small Multi-Use Hood

    FDA UDI
    ACCUTRON, INC.·00813830021523·

    Pathfinder Small Multi-Tool Instrument Clamp

    FDA UDI
    ANALOGIC CORPORATION·90814277020066·

    AMPLATZER MULTI-FENESTRATED SEPTAL OCCLUDER - CRIBRIFORM

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code MLV·September 20, 2022

    MULTI-ACCESS CATHETER

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH, INC.·Product code BSY·August 2, 2016

    2520274-2013-10275

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code NKB·February 19, 2013

    2520274-2013-10914

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNI·February 26, 2013

    2520274-2013-10321

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·February 19, 2013

    2520274-2013-10328

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·February 19, 2013

    2520274-2013-10327

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·February 19, 2013

    2520274-2013-10313

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·February 19, 2013

    2520274-2013-10915

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNI·February 26, 2013

    2520274-2013-10921

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNI·February 26, 2013

    2520274-2013-10338

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·February 20, 2013

    2520274-2013-10306

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·February 19, 2013

    TIBIAL IMPACTOR

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code HWA·September 13, 2007