BEUDAMED
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    Stradis Medical, LLC

    FDA UDI
    STRADIS MEDICAL LLC·M752OHI10000·Carpal Tunnel Kit

    OHI 540

    FDA Adverse Event
    Injury ·OHIO MEDICAL INSTRUMENT CO., PEDIGO PRODUCTS, INC.·Product code FPO·March 18, 2009

    TRI-LOCK BPS SZ 0 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 7, 2017

    IMPLANTABLE NEURO STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·June 21, 2018

    COMPACT WRISTS BLOOD PRESSURE MONITOR

    FDA Adverse Event
    Injury ·OMRON HEALTHCARE, INC.·Product code DXN·April 23, 1999

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code IOR·September 29, 2014

    GN Otometrics A/S

    FDA UDI
    Natus Medical Denmark ApS·05713315005534·1081 AURICAL (PMM, C&S) w/o HI-PRO (US only)

    INTERSTIM X

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·May 17, 2024

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·June 22, 2018

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·December 11, 2014

    SUPERFLEX ASPHERIC

    FDA Adverse Event
    Injury ·RAYNER INTRAOCULAR LENSES LIMITED·Product code HQL·December 10, 2014

    4 FR. S/L POWERPICC - NURSING FULL (TLS)

    FDA Adverse Event
    Injury ·C. R. BARD, INC. (BASD)·Product code LJS·June 1, 2011

    ESSURE

    FDA Adverse Event
    Injury ·CONCEPTUS·Product code HHS·September 18, 2013

    PEN NEEDLE AUTOSHIELD DUO 30GX5MM EU

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·January 15, 2025

    APEX

    FDA Adverse Event
    Malfunction ·APEX DYNAMICS HEALTHCARE PRODUCTS·Product code IKX·September 15, 2012

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·October 1, 2024

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·December 21, 2020

    BIOTENE ORIGINAL ORAL RINSE (ORIGINAL)

    FDA Adverse Event
    Injury ·KIK CUSTOM PRODUCTS·Product code LFD·June 23, 2022

    ELCA CORONARY LASER ATHERECTOMY CATHETER

    FDA Adverse Event
    Death ·SPECTRANETICS CORPORATION·Product code LPC·May 6, 2026

    PILL CRUSHER

    FDA Adverse Event
    Malfunction ·HEALTH ENTERPRISES·Product code OHY·June 6, 2014