BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    LL-55 (METHAFILCON A) FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ACU-STRAP MOTION SICKNESS BAND

    FDA 510(k)
    FDA Unclassified ·Unknown

    LEAF PATIENT MONITORING SYSTEM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TARGETING ARM T2 PROX. HUM.

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 27, 2012

    HUDSON SINGLE HEATED DUAL LIMB W DRAIN

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code CAG·June 3, 2014

    #5 4:1 CUTTING BLOCK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·February 4, 2013

    PRIDE

    FDA Adverse Event
    Injury ·PRIDE MOBILITY PRODUCTS CORPORATION·Product code ITI·December 30, 2010

    LILLIPUT 2

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·November 3, 2023

    PKG, MARYLAND FORCEPS, CURVED LEFT, P/N 0250080282. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

    FDA Enforcement
    Class II ·Terminated·Stryker Endoscopy·December 24, 2014