BEUDAMED
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    Aerobika OPEP Devive with Manometer

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AGXO

    FDA UDI
    Oticon A/S·05707131285027·H160V2, RITE 312 WL STG AGXO

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100226·THORLAKSON ASPIRATING SPECULUM

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE

    ESI

    FDA UDI
    FTT MEDICAL, INC.·B3961501730·CCF HIRSCHMAN ANOSCOPE, 15/16" DIAMETER x 4" LO...

    Tibial Keel Punch : SIZE 3

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215056995·

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 21, 2017

    BD VACUTAINER® K2 EDTA (K2E) PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 29, 2022

    IYUNNI 3ID TRI-FUNNEL FEEDING TUBE KIT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EMS AIR-FLOW MASTER PIEZON

    FDA 510(k)
    FDA Class 2 ·Dental

    POWERPACK

    FDA Adverse Event
    Malfunction ·ICC-NEXERGY·Product code IYN·September 3, 2013

    STRAIGHT TIP T25 DRIVER-LONG

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HXX·June 6, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 6, 2011

    SYNCHROMED II

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·September 3, 2008

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019