BEUDAMED
    33 results · 23ms · Sources: EU EUDAMED, US FDA

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    IO Expandable Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERSALOK

    FDA UDI
    Medos International Sàrl·10886705001163·Versalok Anchor with Threader Tab

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707080862·DISTAL END CUTTER W/SAFETY HOLD CLASSIX

    TALOS®-C HA

    FDA UDI
    MEDITECH SPINE, LLC·B167522108000·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16721312108000·

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345023857·BAYONETTED OSTEOTOME - 1/4"

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197059183·BABCOCK vein probe 80.0 c...

    VERSYO.COM

    FDA 510(k)
    FDA Class 2 ·Dental

    META-LOCK SUTURE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 29, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 8, 2013

    I-STAT 6+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·September 28, 2021

    MITEK VERSALOK TI ANCHOR, THREADER TAB W/O SUTURE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code HWC·March 29, 2012

    VERSALOK ANCHOR WITH THREADER TAB

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HWC·September 4, 2019

    Maquet Coronary Perfusion Cannulae with Balloon Tip, with either self-inflating balloon tip or cone distal tips, straight or right angle, available with proximal end fittings for either 1/4 inch connector or male luer fitting, Model numbers 210800, 210801, 210802, 210803, 210804, 210805, 210806, 210807, 210810, 210811, 210812, 210813, 210814, 210815, 210816, 210817, 215800, 215802, 215803, 215804, 215805, 215806, 215807, 215810, 215811, 215812, 215813, 215814, 215815, 215816, and 215817.

    FDA Recall
    Terminated ·Maquet Cardiovascular·Product code DWF·May 19, 2009

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 15, 2016

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 15, 2016

    VERSALOK THREADER TAB *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HWC·September 20, 2019

    VERSALOK THREADER TAB *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HWC·April 26, 2021