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

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    0.5ml Sol-Care Retractable Safety Syringe with Fixed Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741620300·

    MEGA SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809763501005·Long-Arm Screw Driver

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674162030060·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321620300·

    OMNIBotics

    FDA UDI
    Omni Life Science, Inc.·00841690195368·3.5mm Hex Driver

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L162030120·16mm H x 20mm W x 30mm L XLIF Trial 12 degree L...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138302·Broach, 30 X 26, 15mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138319·Broach, 30 X 26, 17mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138296·Broach, 30 X 26, 13mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138333·Broach, 30 X 26, 21mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138326·Broach, 30 X 26, 19mm Height 16° Hyperlordotic

    SYNTHES RADIAL HEAD PROSTHESIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    US SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    PROSTHESIS, ELBOW, HEMI-RADIAL, POLYMER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code KWI·January 25, 2017

    BLUNT TIP SCREW, ÿ 4X38MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·February 5, 2026

    SYNERGY?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 10, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 6, 2013

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 12, 2011

    M2A 1 PC SHELL 38MMX48MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 30, 2018