BEUDAMED
    160 results · 25ms · Sources: EU EUDAMED, US FDA

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    Acuity 100 (hexafocon A) Rigid Gas Permeable Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    APEX Knee System

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

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111046773·S E METZ SCISS STR DEL 7 TC

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613045531·Instrument Guards, Clear, 3/16" (5mm) x 1" (25....

    Liberty SI

    FDA UDI
    Spinal Simplicity, LLC·M9432001620050·Short Guidewire, Trocar Sharp

    Drill Pin Driver

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215041267·

    Avalign

    FDA UDI
    Avalign Technologies, Inc.·00190776021788·Keyhole Bracket

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776116293·Keyhole Bracket

    II Ring Retractor

    FDA UDI
    Automated Medical Products Corp.·00810118342417·St. Mark’s Retractor 5" with Lip

    PORTEX EPIDURAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ALLURA XPER OR TABLE SERIES

    FDA 510(k)
    FDA Class 2 ·Radiology

    ROSS PATROL

    FDA Adverse Event
    Injury ·ROSS LABORATORIES·Product code LZH·August 17, 2005

    DISTAL FEMUR SMILES SMALL

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE·Product code KRO·December 23, 2016

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQE·June 16, 2006

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376667713·12mm CORE, NANOTEC BAN 16 x 20 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376668123·12mm CORE, NANOTEC KBN 16 x 20 mm 5°

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·February 1, 2006

    UNKNOWN J & J LCS KNEE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·January 27, 2006

    POWER SUPPLY/BATTERY CHARGER

    FDA Adverse Event
    Malfunction ·ELPAC·Product code ITX·June 25, 2010

    PRISMA CONTROL UNIT

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code KDI·October 21, 2005