BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    SYNCHRON SYSTEMS DRUG CALIBRATION 3 PLUS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902974502·INSTRUMENT 6971287 IMP TRIAL 7X18MM

    Sporview VH202 BI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND DEVICE, MODEL SDU-2200PRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACCESS SARS-COV-2 IGM

    FDA Adverse Event
    Malfunction ·CLARE DISCRETE MFG IO·Product code QKO·April 7, 2021

    ACCESS SARS-COV-2 IGM

    FDA Adverse Event
    Malfunction ·CLARE DISCRETE MFG IO·Product code QKO·February 22, 2021

    ACCESS SARS-COV-2 IGM

    FDA Adverse Event
    Malfunction ·CLARE DISCRETE MFG IO·Product code QKO·February 15, 2021

    MALLINCKRODT

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO·Product code BTR·June 30, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 26, 2011

    PUMP MMT-522NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code OYC·November 16, 2007

    ACCESS 2 IMMUNOASSAY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·March 10, 2021

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology