BEUDAMED
    7 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.

    SPECTEF PROTOCOL

    FDA 510(k)
    FDA Class 2 ·Radiology

    ADJUSTABLE PEEP VALVE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MANAN PRO-MAG AUTOMATIC BIOPSY DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TFNA HELICAL BLADE 105MM STERILE

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·March 17, 2017

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 11, 2013

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    LAMITRODE S8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 16, 2014