BEUDAMED
    23 results · 19ms · Sources: EU EUDAMED, US FDA

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    CanGaroo Neuro Envelope (small) ; CanGaroo Neuro Envelope (medium) ; CanGaroo Neuro Envelope (large) ; CanGaroo Neuro Envelope (extra large)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741822550·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674182255060·

    PROPELLER HEAD SCREW SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304269804·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1822550·18mm H x 22mm W x 55mm L x 0 degrees XLIF

    SSW CARBIDE

    FDA UDI
    Ss White Burs, Inc.·D6901822552·GREAT WHITE GOLD CARBIDE GWSL 1557 - 5 PACK

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122292·Kwire .070X9" (1.8x225mm)

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515027046·Sofield Retr, 3/4x4", length 8 3/4"

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L182255120·18mm H x 22mm W x 55mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X182255120·18mm H x 22mm W x 55mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X18225580·18mm H x 22mm W x 55mm L x 8 degrees XLIF

    DMP ETCHING GEL

    FDA 510(k)
    FDA Class 2 ·Dental

    QUADSCAN 4000 BODY BODY COMPOSITION, FLUID & ILLNESS/SEGMENTAL MONITORING UNIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LOCKING SCREW, FULLY THREADED 5X50 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 14, 2010

    LOCKING SCREW, FULLY THREADED 5X50MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·August 24, 2010

    COOK CVC TRIPLE LUMEN POWER-INJECTABLE CENTRAL VENOUS CATHETER TRAY

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·October 21, 2024

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. CRMD·Product code NVN·January 13, 2014

    LANDMARX EVOLUTION

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·July 12, 2011

    AUTOPULSE¿ RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION INC·Product code DRM·June 21, 2013

    BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·June 8, 2021