BEUDAMED
    322 results · 22ms · Sources: EU EUDAMED, US FDA

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    Safe-Cam Tablet and Accessories

    FDA UDI
    BIOTEX, INC.·M710NDK2·

    Smart VIdeo-Stylet Monitor

    FDA UDI
    SMART VIDEO-STYLET, LLC·B881SSCNDK0·Monitor with connecting and re-charging cables,...

    UNK - CONSTRUCTS: EX-FIX

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NDK·April 9, 2021

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code NDK·June 7, 2007

    X-WIRE

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code NDK·June 18, 2007

    EXTERNAL FIXATOR DEVICE

    FDA Adverse Event
    Injury ·UNK·Product code NDK·September 15, 2014

    X-WIRE 2X450MM

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code NDK·October 4, 2006

    STRAIGHT ATTACHMENT ARM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    KLS

    FDA Adverse Event
    Malfunction ·KLS MARTIN L.P.·Product code NDK·January 22, 2001

    5.0MM SELF DRILL SCHANZ SCREW, 200MM, SS

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    CARBON ROD, 450MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    CARBON ROD, 450MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    STRAIGHT ATTACHMENT ARM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    5.0MM SELF DRILL SCHANZ SCREW, 200MM, SS

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    5.0MM SELF DRILL SCHANZ SCREW, 175MM, SS

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    CARBON ROD, 450MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    MULTI-PIN CLAMP, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    5.0MM SELF DRILL SCHANZ SCREW, 175MM, SS

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    MULTI-PIN CLAMP, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    STRAIGHT ATTACHMENT ARM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 21, 2026