BEUDAMED
    26 results · 32ms · Sources: EU EUDAMED, US FDA

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    ULTRA CATHETER SET

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001115·artVeneer life upper anteriors, IS, A35

    4001 115

    Device
    EU MDR · Eu Md Class 1 ·VOE , S.A·On the market

    3001 115

    Device
    EU MDR · Eu Md Class 1 ·VOE , S.A·On the market

    Immunalysis

    FDA UDI
    IMMUNALYSIS CORP·00840937107973·cTHC Urine Calibrator 1

    ClearView

    FDA UDI
    Modus Medical Devices Inc·G34350011151·Clearview 15cm kit - pkg of 4 (500-1115 x4)

    ClearView

    FDA UDI
    Modus Medical Devices Inc·G34350011150·ClearView Dosimeter - 15cm (3L)

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528104262·InstaFix Instrument Kit, 1.5mm

    ELECSYS THYROGLOBULIN CALCHECK

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    RETIC CHEX LINEARITY

    FDA 510(k)
    FDA Class 2 ·Hematology

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    SUREFIT DUAL DISPERSIVE ELECTRODE

    FDA Adverse Event
    Other ·CONMED CORPORATION·Product code DRX·July 13, 2010

    VITALITY

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·August 14, 2008

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013