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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    E-Z DERM BIOSYNTHETIC WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122765·K-WIRE - SINGLE TROCAR THREADED 1.8mm DIA x 230mm

    BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERILETX POWDER FREE LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·December 7, 2010

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 15, 2014

    AFFINITY 3 BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code HDD·December 21, 2012