BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867523883·Spine Compression Screw, 5.0x24mm

    MARQUEST QC-IV TONOMETER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BAKER CKMB REAGENT SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    WALKMED® 150 ML RESERVOIR BAG

    FDA Adverse Event
    Malfunction ·WALKMED TECHNOLOGIES, LLC·Product code FRN·September 5, 2025

    C-QUR V-PATCH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code FTL·June 2, 2014

    LD304 MATERNITY BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV·Product code HDD·October 13, 2010

    UNKNOWN DEPUY ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·December 17, 2012