BEUDAMED
    161 results · 22ms · Sources: EU EUDAMED, US FDA

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    PORTEX EPIDURAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    T-Plate, 2 x 3-Hole

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665027181·

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0620000·Universal Removal Set

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0120050·Screw Sizing Block

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190615·Sizing Guide 3 deg Rotation Bushing -2mm

    Symmetry Hudson (Ewald)

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482052075·Symmetry® Forceps, Hudson, 1x2 Teeth, 4 3/4 in

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694016377·CMF Auxiliary Instrument Tray

    MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BOLUSPRO ULTRA

    FDA 510(k)
    FDA Class 2 ·Radiology

    ZIMMER FEMORAL HEAD 6 DEGREE TAPER

    FDA Adverse Event
    Injury ·ZIMMER CARIBE·Product code JDI·July 29, 2005

    HNM Medical

    FDA UDI
    HNM STAINLESS, LLC.·00842962107959·HUDSON FORCEPS, 4 3/4", 1X2 TEETH

    NUCLUES 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·June 8, 2005

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·*·Product code GDW·July 21, 2005

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·*·Product code GDW·July 21, 2005

    SYNCHROMED EL

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC., NEUROLOGICAL DIV·Product code LKK·July 5, 2005

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code LXH·November 11, 2005

    ICD LEAD 1581

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code LWS·September 20, 2005

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·July 22, 2005

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·March 23, 2006

    REPLACE SELECT TAPERED TIU RP 4.3 X 16MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE USA, LLC.·Product code DZE·July 21, 2005