BEUDAMED
    9 results · 20ms · 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 ×

    POWDER FREE SYNTHETIC EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ENDOPATH ENDOSCOPIC LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·February 19, 1997

    POST-AURICULAR HEARING AID HC 880

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Clarity Reveal

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPIROPERFECT

    FDA Adverse Event
    Malfunction ·MEDIKRO OY·Product code BZG·August 11, 2023

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2013

    FINELINE II

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code DTB·July 31, 2014

    SPRINT QUATTRO

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·January 27, 2011

    ENDOPATH ENDOSCOPIC LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·EES-CINCINNATI·Product code GAG·February 20, 1997