BEUDAMED
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    KARL STORZ REMORGIDA FORCEPS

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

    OMNIBotics

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

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111154·FOX EYE SHIELD GARTER ASST COLOR PK/50

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110980·STERILIZING CASE PLASTIC LARGE

    US SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    0.5ml Sol-Care Retractable Safety Syringe with Fixed Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BONE SCREW DRILL 3.2 MM DIAMETER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWT·August 26, 2020

    NexGen® Legacy® Prolong®

    FDA UDI
    Zimmer, Inc.·00889024211049·

    NexGen® Complete Knee Solution

    FDA UDI
    Zimmer, Inc.·00889024665880·

    NexGen® Complete Knee Solution

    FDA UDI
    Zimmer, Inc.·00889024665897·

    NexGen® Complete Knee Solution

    FDA UDI
    Zimmer, Inc.·00889024665903·

    NexGen® Complete Knee Solution

    FDA UDI
    Zimmer, Inc.·00889024665873·

    NexGen® Legacy® Prolong®

    FDA UDI
    Zimmer, Inc.·00889024211056·

    NexGen® Legacy® Prolong®

    FDA UDI
    Zimmer, Inc.·00889024211018·

    NexGen® Legacy® Prolong®

    FDA UDI
    Zimmer, Inc.·00889024211025·

    NexGen® Legacy® Prolong®

    FDA UDI
    Zimmer, Inc.·00889024211063·

    NexGen® Complete Knee Solution

    FDA UDI
    Zimmer, Inc.·00889024665866·

    NexGen® Legacy® Prolong®

    FDA UDI
    Zimmer, Inc.·00889024211032·

    NexGen® Complete Knee Solution

    FDA UDI
    Zimmer, Inc.·00889024665910·

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·February 14, 2013