BEUDAMED
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    FEMORAL NAIL, LEFT 10X380 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·July 22, 2011

    ARROW CVC SET: 4-LUMEN 8.5FR X 16CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQY·October 14, 2020

    ARROW CVC SET: 4-LUMEN 8.5FR X 16CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQY·October 13, 2020

    TARGET DEVICE T2 GTN

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·October 10, 2012

    GUIDE WIRE, BALL-TIPPED, STERILE T2 HUMERUS Ø2.5X800 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·August 6, 2014

    VOLUMAT MC AGILIA AUS

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S.·Product code FRN·March 13, 2025

    VOLUMAT MC AGILIA AUS

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S.·Product code FRN·March 13, 2025

    GUIDE WIRE, BALL-TIPPED 2.5X800 MM

    FDA Adverse Event
    Other ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 30, 2011

    PROXIMATE*PPH PROCEDURE SET

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 27, 2019

    END CAP, STANDARD T2 TIBIA Ø8 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL (MDR)·Product code HSB·August 18, 2015

    UNKNOWN TARGET DEVICE

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·January 24, 2018

    RADIOLUCENT DRIVE DRILL BIT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code GFG·January 7, 2016

    DIAMONDBACK 360 CORONARY ORBITAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Injury ·CARDIOVASCULAR SYSTEMS, INC.·Product code MCX·June 30, 2022

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X55 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·March 27, 2014

    FEMORAL NAIL, LEFT T2 GTN Ø8X300 MM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code HSB·March 3, 2025

    DRILL, TRI-FLAT T2 FEMUR Ø4,2X340 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·March 25, 2013

    FEMORAL NAIL, LEFT T2 GTN Ø11X420 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·March 27, 2014

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X45 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·March 27, 2014

    AGENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·January 13, 2021

    ARROW CVC SET: 4-LUMEN 8.5FR X 16CM

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC.·Product code DQY·January 4, 2021