BEUDAMED
    8 results · 30ms · 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.

    APLICARE ONE COMPUND BENZION TINCTURE SWABSTICK

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ERA 2.2MM ANGLE IMP MICRO HEAD 15X3MM ACID ETCH, Ti

    FDA UDI
    STERNGOLD DENTAL LLC·00841549115660·Designed for both transitional and long-term de...

    ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MTS SYSTEM, WIDE-SPACE QUATTRODE PERCUTANEOUS LEADS

    FDA 510(k)
    FDA Class 2 ·Neurology

    BUCKY DIAGNOST

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code KPR·November 2, 2010

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    PALL TRANSFER/FREEZING BAG SET

    FDA Adverse Event
    Malfunction ·PALL MEDSEP·Product code KSR·October 5, 2006

    Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015