BEUDAMED
    11 results · 19ms · 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 ×

    Self-adhesive Electrode

    FDA 510(k)
    FDA Class 2 ·Neurology

    LCP

    FDA UDI
    Synthes GmbH·10886982156853·LCP(TM) DISTAL FEMUR PLATE 7 HOLES/196MM-RIGHT

    STERNGOLD 1, MODEL 1127781

    FDA 510(k)
    FDA Class 2 ·Dental

    SPACE CHAMBER PLUS COMPACT SPACE CHAMBER PLUS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE, INC.·Product code OUR·March 22, 2019

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE, INC.·Product code OUR·October 24, 2019

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 24, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 3, 2014

    LTC MED SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·July 12, 2013

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·August 20, 2024

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·November 18, 2024