BEUDAMED
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    Disposable Pneumatic Vitrectome.(20 gauge / 0.9 mm)(working with 30 P.S.I., max.

    FDA UDI
    D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.·08717872001395·

    Nevadent

    FDA UDI
    Inwood Electronic Co., Ltd·16974637100017·

    Hydrafacial Syndeo

    FDA UDI
    Hydrafacial LLC·00810007533711·100 –120VAC, 50/60Hz, 2A

    Hydrafacial Syndeo

    FDA UDI
    Hydrafacial LLC·00810007533605·220-240VAC, 50/60Hz, 2A

    NMD SURGICAL LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·November 18, 2010

    VPAP III ST - ASIA PACIFIC

    FDA Adverse Event
    Injury ·RESMED LTD.·Product code BZD·January 28, 2011

    PROSTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MDI·April 20, 2014

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·December 27, 2019

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·December 27, 2019

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·December 27, 2019

    PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code LGW·April 26, 2024

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES(USA)·Product code HWC·May 15, 2014

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 17, 2014

    RHYTHMIA HDXTM MAPPING SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NMD·July 29, 2024

    RHYTHMIA HDXTM MAPPING SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NMD·August 14, 2024

    PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·November 13, 2024

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·February 27, 2015

    OCTRODE LEAD

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·January 3, 2024

    PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·May 19, 2025

    PENTA 3MM LEAD, 60 CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·March 14, 2025