BEUDAMED
    24 results · 24ms · Sources: EU EUDAMED, US FDA

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    MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM / TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION SYRINGE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    n/a

    FDA UDI
    HANS RUDOLPH, INC.·00874750006083·2300 2W NRBV T MINI FELUER MP

    24PW - PG&E - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588120867·24PW - PG&E - Poly White

    TLIF/PLIF Disc Prep

    FDA UDI
    Life Spine, Inc.·00190837087005·

    Integrity-SI Fusion System

    FDA UDI
    Lincotek Medical LLC·B57112521112086D0·12 x 85 mm SI Implant Fully Threaded with HA Co...

    AQUARIUSNET SERVER

    FDA 510(k)
    FDA Class 2 ·Radiology

    ELECSYS CA 125 II CALCHECK 5

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·February 24, 2014

    AWL Ø2 ANGL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVE·January 8, 2013

    AWL Ø2 ANGL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVE·January 7, 2013

    AWL Ø2 ANGL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVE·January 7, 2013

    EMG TUBE 8229737 3PK NIM TRIVANTAGE 7MM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·November 12, 2014

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 7, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·June 2, 2011

    IN TOUCH ZX

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL QUEBEC·Product code FNL·August 6, 2008

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·July 19, 2016

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·January 14, 2015

    CAROTID WALLSTENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIM·December 15, 2023

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·August 15, 2016

    NIM® PROBE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·March 23, 2018