BEUDAMED
    18 results · 28ms · Sources: EU EUDAMED, US FDA

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    LEGION COBALT CHROME REVISION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GII ARTICULAR INSERTER/EXTRACT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018

    MOSS MIAMI 5.5MM TITANIUM PIN NUT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES ANTERIOR CSLP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROSPACE PEEK IMPLANT 5 7X8X22MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code MAX·June 21, 2013

    BD ULTRASAFE X100L PR CLEAR SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·July 26, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·September 26, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·August 21, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·April 24, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·October 3, 2019

    TSPACE PEEK IMPLANT 26X11X7MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code MAX·October 30, 2015

    5.0 CM SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·April 5, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·April 6, 2011

    PUMP MMT-522WWP PRDGM INSULIN PL EN ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LZG·June 11, 2008

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·August 23, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·March 28, 2019

    ULTRASAFE X100L PR GREY SSL SDZ

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·September 11, 2019

    Ondamed Biofeedback Device, Model No. 001-00-0101 The product is a battery powered biofeedback device that is indicated for relaxation training and muscle re-education and prescription use.

    FDA Enforcement
    Class II ·Terminated·Ondamed Inc·May 16, 2018