BEUDAMED
    31 results · 21ms · Sources: EU EUDAMED, US FDA

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    ACCUMAP AUTOMATIC PERIMETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    Woven Filiform Coude Tip

    FDA UDI
    C. R. Bard, Inc.·00801741073236·Woven Filiform Coude Tip

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694000437·2.3mm x 4mm Safety Screw

    2040 Ceramic Brackets

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746005626·COSMETIC 20/40 UL LAT 018 T+10 A+8 R=0

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776308018·Bi-Manual Asp HP 23g .4mm single port cvd

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694062688·2.0 System x 4mm Emergency Screw Sterile Qty 2

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981157128·Cambria Trial without Depth Stop

    DISPOSABLE LIGHT HANDLE AND ADAPTOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ADC 656 ELECTRONIC STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PYRENEES® Cervical Plate System

    FDA UDI
    VB Spine LLC·10888857241930·Anti-Torque Guide, Translational

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 27, 2025

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 2, 2024

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·September 11, 2024

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 27, 2013

    RADIAL JAW 4 BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·March 17, 2011

    LIBERTE' MONORAIL CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code MAF·March 26, 2008

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·March 13, 2024

    ANGLED REAMER SLEEVE, 10°

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·September 3, 2023

    ANGLED REAMER SLEEVE, 10°

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 3, 2024

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 3, 2024