BEUDAMED
    12 results · 26ms · Sources: EU EUDAMED, US FDA

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    STERRAD 100NX Sterilizer with ALLClear Technology

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153171157·TENSION PLIERS 1.7MM, MID-FACE

    AXS

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327369458·AXS SCREWDRIVER BLADE 1.2/1.7MM

    CADD

    FDA UDI
    ICU MEDICAL, INC.·15019517139075·

    ONE TOUCH ULTRASMART

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·February 15, 2005

    ERIS LAYERING MATERIALS

    FDA 510(k)
    FDA Class 2 ·Dental

    NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN_FRO_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code JEY·October 12, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 29, 2014

    LTV

    FDA Adverse Event
    Malfunction ·CAREFUSION 203, INC·Product code CBK·July 8, 2011

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 8, 2013

    Model Number L211 PROPONENT DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025