BEUDAMED
    25 results · 22ms · Sources: EU EUDAMED, US FDA

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    ERGOSELECT/GE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    McKesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·20612479174799·Lab Sponges X-RAY DETECTABLE STERILE| 4 PLY| 10...

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08806390852357·

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089436170·

    SECUREGUARD RETRACTABLE SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ECLIPSE VERTEBRAL SPACER SYSTEM-LUMBAR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089436163·

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089436149·

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089436156·

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·January 18, 2019

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·January 18, 2019

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 4, 2022

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 23, 2014

    INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·June 19, 2006

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 2, 2011

    UNKNOWN SCREW

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

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 25, 2022

    McKesson Lap Sponge, X-Ray Detectable 12"x 12", 5/pack, Sterile McKesson Part # 16-2112121

    FDA Recall
    Terminated ·Cypress Medical Products LLC·Product code GDY·August 11, 2021

    McKesson Lap Sponge, X-Ray Detectable 12"x 12", 5/pack, Sterile McKesson Part # 16-2112121

    FDA Enforcement
    Class II ·Terminated·Cypress Medical Products LLC·September 22, 2021