BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    TUBING PACK, EXTRACORPOREAL, H-3000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515200302·Bone Awl, 5 1/2"

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471184806·.022 U/L Std. Comb. Weld Size#20

    NA

    FDA UDI
    aap Implantate AG·04042409262234·Handle with quick coupling, with torque limiter...

    MON-A-THERM TEMPARATURE MONITOR SYS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Portex Blue Line Ultra Paediatric Tracheosomy Tube

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HOLLYWOOD NM IMPLANT, 11MMX27MMX8MM, LORDOIC

    FDA Adverse Event
    Malfunction ·SEASPINE, INC.·Product code NKB·February 18, 2014

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·October 1, 2012

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·September 5, 2007

    Safety glasses made with "Rage" frames manufactured between February 20, 2014 and February 25, 2014. The color of the frames of the recalled glasses were either white or black. Safety Eye wear

    FDA Recall
    Terminated ·Wal Mart Stores, Inc·Product code HQG·February 26, 2014