BEUDAMED
    12 results · 19ms · 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.

    -OM WEST 2000 GNATUS CHAIR

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Shoreline™ ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981142674·Trial Rasp, 14x13x8mm, 7 Deg Lordosis

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197511896·Balfour Hogan central blade 50x127...

    HEALTH CHECK KIOSK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CareLink SmartSync Device Manager - Pacing System Analyzer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EQUINOXE REVERSE HUMERAL ADAPTER TRAY

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 6, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 9, 2010

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 10, 2012

    G7 SCREW 6.5MM X 20MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 6, 2017

    G7 SCREW 6.5MM X 20MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 6, 2017

    G7 SCREW 6.5MM X 20MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 6, 2017

    G7 OSSEOTI MULTIHOLE 54MM F

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·June 6, 2017