BEUDAMED
    14 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 ×

    MECHANICAL TABLES AND ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    N/A

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490047241·DRILL 1882900 MINI TREPHINATION 2MM

    Reprocessed 2.0mm Mini Trephination Drill

    FDA UDI
    SURETEK MEDICAL·B39018829001·Reprocessed 2.0mm Mini Trephination Drill, Open...

    KYMCO FORU, MODEL EQ10

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    3880 MRI Patient Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DRILL 1882900 MINI TREPHINATION 2MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·January 16, 2013

    DRILL 1882900 MINI TREPHINATION 2MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·April 18, 2013

    DRILL 1882900 MINI TREPHINATION 2MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·December 9, 2013

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code OZO·December 12, 2020

    XPS® BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·July 1, 2016

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 4, 2014

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·October 22, 2010

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 21, 2012

    XPS® BLADE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code EQJ·July 24, 2015