BEUDAMED
    10 results · 18ms · 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 ×

    MED-E-JET INJECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EBERLE

    FDA UDI
    Eberle GmbH & Co. KG·04050052020132·Universal handpiece

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO·Product code DWJ·December 23, 2010

    REAADS ANTI-PHOSPHATIDYLSERINE IGA SEMI-QUANTITIVE TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    APOLLO V+ MEDICAL PLATFORM, APOLLO IV+ MEDICAL PLATFORM, NICE STATION LIGHT BASED PLATFORM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 22, 2016

    WARM TOUCH II COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DWJ·September 24, 2010

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·January 14, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 14, 2014

    AMS 700 INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code JCW·November 19, 2010