BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    IRRIGATION/ASPIRATION TUBING SET

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ACUFEX PASSING PINS AND SURGICAL WIRE

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    ELLIPSE 2.3

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    LOCKING SCREW, FULLY THREADED 5X50 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 14, 2010

    LOCKING SCREW, FULLY THREADED 5X50MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·August 24, 2010

    UNK JUVEDERM VOLUMA

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·June 17, 2014

    HOSPITAL FULL FACE NON-VENTED MASK

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code MNT·January 22, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIV·Product code FNL·November 23, 2010

    Halogen Lamp component in RetCam 3 System - Clarity Medical Systems, Inc; Pleasanton, CA. General ophthalmic imaging including retinal, corneal and external imaging. Photo-documentation of pediatric ocular diseases including retinopathy of prematurity. Screening for Type-2 re-threshold retinopathy of prematurity or treatment requiring ROP.

    FDA Recall
    Terminated ·Clarity Medical Systems Inc·Product code HKI·March 7, 2014