BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    TEETHMATE-F

    FDA 510(k)
    FDA Class 2 ·Dental

    Nexxis OR

    FDA UDI
    Barco NV·05415334042346·NEXXIS WORKSPOT KIT2 CM

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756352017·BASIC PACK

    DIGNITY MINI PORT- ATTACHABLE; DIGNITY MINI PORT- PRE ATTACHED; DIGNITY LOW PROFILE PORT- ATTACHABLE; DIGNITY LOW PROFIL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEXAN SYSTEM, MODEL NX-301

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN RIGHT HIP NECK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·January 8, 2013

    SYMBIQ SINGLE CHANNEL

    FDA Adverse Event
    Injury ·HOSPIRA, INC.·Product code FRN·November 18, 2010

    MARATHON MICRO CATHETER

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code DYG·July 2, 2014

    FASTPAK batteries labeled Manufactured for Medtronic Physio-Control 11811 Willows Rd, Redmond, WA USA. Batteries are Nickel-Cadmium (NiCd) battery packs used to provide DC power to LIFEPAK 5, 10, 11, or 12 defibrillator/monitors. The FASTPAK battery has a capacity of 1 amp/hour (1.0AH). The FASTPAK battery can be charged in a Battery Support System, Battery Support System 2, Mobile Battery Service Station, or the LIFEPAK 10, 11 or 12 defibrillator/monitor when the device is powered by an external power adapter. The FASTPAK battery does not have a pushbutton fuel gauge like the LIFEPAK NiCd. The fuel gauge provides a visual indication of battery capacity. Battery part number 9-10424-18. Sold with LIFEPAK defibrillators and also sold separately.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·February 27, 2008