BEUDAMED
    8 results · 28ms · 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.

    HARE EMERGENCY STRETCHER WITH WHEELS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CLASSIC BAG SIZE 1 200 PCS

    FDA UDI
    PaloDEx Group Oy·06430035873258·

    Lower ROC Pack for Herbst LL4 8mm

    FDA UDI
    SPECIALTY APPLIANCES, LLC·D8199006710·

    PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDERED LATEX EXAM GLOVES, PINK, WITH/WITHOUT STRAWBERRY SCENT, PROTEIN LABELING

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ACS POLY W/ 10 LIP 32 GR2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JDI·June 27, 2014

    PRISM HTLV-I/HTLV-II

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code MTP·November 16, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 8, 2013