BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    MRP-7000/AIRIS QD C-SPINE COIL (P/N MR-QCSC-42,MR-QCSC-52)

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALIF

    FDA UDI
    Nuvasive, Inc.·00887517691125·ALIF Bullet Distractor, 16mm 10°

    NA

    FDA UDI
    KEY SURGICAL, INC.·00849771048220·K-Wire and Steinmann Pin Dispensers, .062-inch...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292336·DISP K-WIRE FOR .062" (1.6MM) 12.25"

    K-Wire and Steinmann Pin Dispensers

    FDA UDI
    KEY SURGICAL, INC.·00849771012054·K-Wire and Steinmann Pin Dispensers, .062-inch...

    INTERMEDULLARY BRUSH

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DEPUY RESTORE ORTHOBIOLOGIC SOFT TISSUE IMPLANT

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

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024214651·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024214644·

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWP·August 5, 2015

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·January 6, 2011

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 8, 2014