BEUDAMED
    9 results · 25ms · 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.

    AESCULAP ACCU-DERMATOME

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Everest & Jennings

    FDA UDI
    GF HEALTH PRODUCTS, INC.·M36889402081·DURA-GEL SPP-AT

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123021·K-WIRE - SINGLE TROCAR 2.0mm DIA x 200mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867524255·ECLIPSE CAGE SCREW SIZER

    NEPTUNE PAD, NEPTUNE DISC, NEPTUNE COMFORT-BAND, COMFORT-BAND

    FDA 510(k)
    FDA Unclassified ·Unknown

    FERM-FLEX AND FEM-FLEX II ( FEMORAL ACCESS ARTERIAL CANNULAE) FEMTRAK,VFEM, AND FEM-FLEXII

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ICY HOT SMART RELIEF TENS THERAPY

    FDA Adverse Event
    Injury ·CHATTEM, INC.·Product code NUH·June 19, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 23, 2010