BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    ORTHOBLAST II PUTTY AND PASTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORTHOBLAST

    FDA Adverse Event
    Injury ·INTEGRA LIFE SCIENCES·Product code MBP·September 27, 2013

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450198674·

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015

    CT LUCIA

    FDA UDI
    CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100638·3-piece, monofocal, hydrophobic, acrylic, intra...

    SOFT K. AND SOFT K. TORIC (XYLOFICON A) SOFT (HYDROPHILLIC) KERATOCONUS CONTACT LENS FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PLEURX PLEURAL CATHETER AND DRAINAGE KITS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC.·Product code GEI·March 14, 2013

    STAIR PRO - MODEL 6251

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·March 14, 2011

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008

    COPELAND THN SHL COCR/HA HUMS3

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·August 28, 2025