BEUDAMED
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    SAS SHIGELLA BOYDII TYPE 13 ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799003690·

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239420·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 3 12.5m...

    SPACE CPSXL BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IntelliVue Patient Monitors MP2, MP5, MP5T, MP5SC, and Multi-Measurement Module X2; IntelliVue Patient Monitors MP20, MP30, MP40, MP50, MP60; IntelliVue Patient Monitors MP70, MP80, MP90;IntelliVue Patient Monitors MX400, MX430, MX450, MX500, MX550, MX600;IntelliVue Patient Monitors MX700, MX800

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PUMP 381 PUMP SET (US)

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·January 19, 2026

    ICC 200

    FDA Adverse Event
    Malfunction ·ERBE USA INCORPORATED·Product code GEI·December 29, 2010

    CURLIN INFUSION 6000 PAINSMART IOD IV PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code FRN·January 17, 2013

    UNKNOWN DEPUY HIP LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code KWA·July 28, 2014