BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 16, 2011

    REFLEXION¿ SPIRAL EP CATHETER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code DRF·August 30, 2018

    "2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·May 18, 2018

    TIBIAL INSERT COMPONENT SIZE 5 GREEN PLUS (+) 0 MM THICKNESS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NTG·February 4, 2022

    IMP,TSV,MCOL MG,3.7MM,13M

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·February 10, 2022

    DISTAL LATERAL FIBULAR PLATE LEFT 6 HOLES 106 MM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWC·February 4, 2022

    TIBIAL BASE COMPONENT SIZE 5 GREEN FOR USE WITH SIZE 5 TALAR COMPONENTS ONLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·February 4, 2022

    STERNALOCK 6 HOLE STRAIGHT PLATE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·July 6, 2015

    UNKNOWN OXFORD FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·June 22, 2020

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·June 22, 2020

    STERNALOCK BLU SYSTEM SCREW, CANCELLOUS CROSS-DRIVE LOCKING 2.4 X 12MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·October 7, 2015