BEUDAMED
    10 results · 21ms · 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 ×

    PCD 737A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    QCT Pro Asynchronous Calibration Module, CliniQCT

    FDA UDI
    MINDWAYS SOFTWARE, INC.·B052DIASYNC0·The QCT Pro Asynchronous Calibration Module is ...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017781·K-Wire, Double Ended, Trocar Point, Diameter Si...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017798·K-Wire, Double Ended, Trocar Point, Diameter 0....

    SILJETR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    LPO OPTION FOR DRAGER INTENSIVE CARE VENTILATOR SAVINA

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 22, 2021

    TENDRIL DX

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DTB·January 13, 2014

    TPS HANDPIECE CORD

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·May 31, 2013

    CORE SUMEX DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·June 17, 2011