BEUDAMED
    28 results · 22ms · 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 ×

    EXTRUDE MODIFIED

    FDA 510(k)
    FDA Class 2 ·Dental

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890124050·Zirlux Shading Liquid - Effects, dark pink, 30ml

    TREK

    FDA UDI
    ABBOTT VASCULAR INC.·08717648153952·TREK Coronary Dilatation Catheter 2.50 mm x 6 m...

    TREK

    FDA UDI
    ABBOTT VASCULAR INC.·08717648153990·TREK Coronary Dilatation Catheter 2.50 mm x 20 ...

    TREK

    FDA UDI
    ABBOTT VASCULAR INC.·08717648154003·TREK Coronary Dilatation Catheter 2.50 mm x 25 ...

    TREK

    FDA UDI
    ABBOTT VASCULAR INC.·08717648153969·TREK Coronary Dilatation Catheter 2.50 mm x 8 m...

    TREK

    FDA UDI
    ABBOTT VASCULAR INC.·08717648153983·TREK Coronary Dilatation Catheter 2.50 mm x 15 ...

    TREK

    FDA UDI
    ABBOTT VASCULAR INC.·08717648153976·TREK Coronary Dilatation Catheter 2.50 mm x 12 ...

    TREK

    FDA UDI
    ABBOTT VASCULAR INC.·08717648154010·TREK Coronary Dilatation Catheter 2.50 mm x 30 ...

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0120050·Screw Sizing Block

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 9, 2015

    SPINAL EPIDURAL NEEDLES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    7230 ULTRASOUND IMAGING SYSTEM WITH TEI

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 13, 2015

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0154051·TRIAL, DRILL GUIDE 14 X 11, 5 MM TA

    EP WORKMATE

    FDA Adverse Event
    Malfunction ·EPMEDSYSTEMS, INC.·Product code DXG·December 24, 2004

    PELORIS RAPID TISSUE PROCESSOR

    FDA Adverse Event
    Injury ·LEICA BIOSYSTEMS MELBOURNE·Product code IEO·March 14, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 9, 2011

    MICROTARGETING DRIVE SYSTEM

    FDA Adverse Event
    Malfunction ·FHC, INC.·Product code HAW·March 14, 2008

    BD SYRINGE 1ML LS 27GA 1/2IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·September 6, 2024