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

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    3 in 1 TENS UNIT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813033906·Hedstrom Files with Silicone Stops 25mm #35

    BIPAP AUTO

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Hyper-C Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIPAP AUTO M-SERIES

    FDA Adverse Event
    Death ·RESPIRONICS, INC·Product code BZD·July 11, 2012

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    BIPAP AUTO BIFLEX

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    BIPAP AUTO SERIES ASSY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 31, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    BIPAP AUTO SERIES ASSY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code BZD·March 31, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 31, 2022

    ACROMIOBLASTER, 4.0 MM, EP-1, DISP BURR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code HTT·December 2, 2008

    AMSCO

    FDA Adverse Event
    Malfunction ·STERIS·Product code FQO·September 8, 2011

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·July 29, 2013

    BIPAP AUTO M-SERIES

    FDA Adverse Event
    Other ·RESPIRONICS INC.·Product code BZD·June 8, 2012

    PATIENT INTERFACE NIM4CPB1 NIM 4.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·October 28, 2025