BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    LOGIQ E

    FDA 510(k)
    FDA Class 2 ·Radiology

    K133532

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 2, 2021

    POWDER FREE LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ES TROCHANTERIC NAIL, LEFT AND RIGHT, 10MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BAXANO IO-FLEX SYSTEM

    FDA Adverse Event
    Other ·BAXANO, INC.·Product code HAE·July 2, 2012

    BAXANO IO-FLEX SYSTEM

    FDA Adverse Event
    Other ·BAXANO, INC.·Product code HAE·July 2, 2012

    BAXANO IO-FLEX SYSTEM

    FDA Adverse Event
    Other ·BAXANO, INC.·Product code HAE·July 2, 2012

    BELT CLIP

    FDA Adverse Event
    Malfunction ·Product code LZG·October 1, 2014

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·May 29, 2013

    ZMR HIP SYSTEM FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC.·Product code LPH·June 15, 2011