BEUDAMED
    7 results · 19ms · 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 ×

    OCTEIA INTACT PTH

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    N LATEX CYSTATIN

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HONGYUN POWDER-FREE YELLOW VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HUDSON SINGLE HEATED DUAL LIMB W DRAIN

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

    TIBIAL PUNCH TOWER ASSEMBLY

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

    SENSOR, MMT-7002C, 10PK,GLUCOSE,BSA, 17L

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·December 22, 2010

    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