BEUDAMED
    11 results · 21ms · 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 ×

    VentStar Helix dual heated (N) Plus (MP02650), VentStar Helix heated (N) Plus (MP02608)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010104205·4.0MM FULLY THREADED CANNULATED ...

    AED

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657006460·Handle, flat

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111200267·PRECISION SUTURE SCI CVD 3 1/2

    Pressure Sentinel®

    FDA UDI
    Zimmer, Inc.·00889024039056·

    Pressure Sentinel®

    FDA UDI
    Zimmer, Inc.·00889024039063·

    SPECTRUM SPINE LAMINOPLASTY PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Helianthus

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·August 6, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 25, 2011

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FNL·July 12, 2013