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

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    OSSEOSPEED ANGLED ABUTMENT EV

    FDA 510(k)
    FDA Class 2 ·Dental

    XLIF

    FDA UDI
    Nuvasive, Inc.·00887517055569·NAV.S XLIF Trial, 12x18mm 10° Lollipop

    XLIF

    FDA UDI
    Nuvasive, Inc.·00887517053961·XLIF AMS Trial, 12x18mm 10° Modular

    MONOPTY

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741084638·MONOPTY® Disposable Core Biopsy Instrument, 22m...

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010064769·4.0MM PARTIALLY THREADED ...

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981265779·Trial, 39mm x 27mm x 18mm, 10 Deg

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981246525·Interbody, 39mm x 27mm X 18mm, 10 Deg

    AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    3DHJD CAMERA SYSTEM MODEL

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NIOX

    FDA UDI
    Circassia AB·07350047030663·Contains One NIOX VERO device, one sensor pre-p...

    Ascendant

    FDA UDI
    Choice Spine, LP·10885862261175·

    BARD MONOPTY DISPOSABLE CORE BIOPSY INSTRUMENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·June 6, 2017

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 21, 2013

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·September 26, 2014

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CGN·May 20, 2011

    MONOPTY DISPOSIBLE NEEDLE

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·July 28, 2015

    EGIA 45 ARTICULATING MED/THICK SULU

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·December 9, 2015

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024