BEUDAMED
    7 results · 19ms · 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 ×

    GYNEX IRIS HOOK, GYNEX ANGLE HOOK, GYNEX EMMETT TENACULUM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    QUIKCLOT NOSEBLEED

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

    DAEHAN Adhesive Surface Electrodes

    FDA 510(k)
    FDA Class 2 ·Neurology

    PALIND 23/40 SLOT SPRT W/VT

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code MSD·February 1, 2013

    SUPER TURBOVAC 90 WITH INTEGRATED CABLE

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code GEI·February 2, 2011

    ZIMMER NATURAL NAIL CM LAG SCREW REAMER

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSB·July 2, 2014

    Angiotech Galactography Kit. Galactography Kit 30ga with Straight Cannula and Galactography Kit 30ga with Curved Cannula. STERILE. Product Number: DGK002SX, DGK002X. 510k K980227. Qty Dist. - 2,630. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended use: Injection Media Contrast Kit Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code FMI·September 1, 2009