BEUDAMED
    46 results · 26ms · Sources: EU EUDAMED, US FDA

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    FLUID PUMP, CP #3

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377069702·RELINE C Screw, 4.5x24mm FA

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867057715·UNI GLENOID-PERIPHERAL LOCK SCRW

    CAPTIA(R) SYPHILIS M, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SURGICAL CLIPPER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    AU680 CHEMISTRY ANALYZER WITH ISE

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·January 14, 2013

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA·Product code NIM·December 3, 2010

    PINN SECTOR W/GRIPTION 54MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 3, 2014

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·December 21, 2020

    UNIVERSAL GLENOID - BASEPLATE SMALL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·December 21, 2020

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·December 21, 2020

    UNIVERSAL GLENOID - BASEPLATE SMALL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

    UNIVERS REVERS GLENOSPHERE 36 +2.5 INF

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 4, 2019

    HUMERAL INSERT S/36 +3 TO FIT IN 36 CUP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

    UNIVERS REVERS SUTURE CUP, 36 (+2 RIGHT)

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSD·April 4, 2019

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

    UNIVERS REVERS HUMERAL STEM, SIZE 6

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSD·April 4, 2019

    1220246-2019-01001

    FDA Adverse Event
    Injury ·April 4, 2019

    HUMERAL INSERT S/36 +6 TO FIT IN 36 CUP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

    1220246-2019-01005

    FDA Adverse Event
    Injury ·April 4, 2019