BEUDAMED
    33 results · 49ms · Sources: EU EUDAMED, US FDA

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    HEARTWAY LIGHTWEIGHT POWER CHAIR, P15

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122155·KWire .028x4" (0.7x100mm)

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0170050·Draw Rod, Wedge

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0310050·Probe, 1.5 inch Ball, Lenke, Curved, Black

    General Instrument

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132127094·Zimmer In-Line Ratchet

    WAKO HDL-C/LDL-C CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PURE WATER SOLUTIONS CENTRAL WATER SYSTEM FOR HEMODIALYSIS

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

    9616026-2006-00240

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616026-2006-00244

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    FULL FACE MASK

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code MNT·March 28, 2008

    ALEUTIAN SPACER, MODEL K2-07-1004-01, K2-07-1005-01

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9616026-2006-00239

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    AVISTA MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 28, 2022

    9616026-2006-00222

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00252

    FDA Adverse Event
    Other ·Product code FII·June 21, 2006

    LINEAR 3-4

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 20, 2021

    9616026-2006-00245

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006