BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Spectralis HRA+OCT and variants with OCT Angiography Module

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780362319·Integra® Miltex® McGuire Corneal Scissors 4-1/8...

    POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEDLINE POWDER-FREE NITRILE EXAMINATION GLOVE WITH ALOE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    TRULIANT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 14, 2025

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    PWRD ECH FLEX 60MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 21, 2013

    STANDARD LOW IMPEDANCE LEAD

    FDA Adverse Event
    Malfunction ·MPROC, VILLALBA·Product code LGW·July 5, 2011

    PULSE GEN MODEL

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 25, 2008