BEUDAMED
    9,062 results · 28ms · Sources: EU EUDAMED, US FDA

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    OPTETRAK TIBIAL INSERT

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code JWH·August 16, 2018

    D-STAT DRY HEMOSTATIC BANDAGE

    FDA Adverse Event
    Injury ·VASCULAR SOLUTIONS, INC.·Product code FRO·April 14, 2011

    OPTETRAK LOGIC FEMORAL COMPONENT, POSTERIOR STABILIZED, CEMENTED

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code JWH·August 16, 2018

    OPTETRAK LOGIC FIT TIBIAL TRAY, CEMENTED

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code JWH·August 16, 2018

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 8, 2008

    SIGMA PLI XLK INS 2 10MM

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DE PUY ORTHOPAEDICS·Product code JWH·February 7, 2008

    DIAMONDBACK CORONARY

    FDA Adverse Event
    Malfunction ·CARDIOVASCULAR SYSTEMS, INC.·Product code MCX·July 22, 2025

    D-STAT FLOWABLE HEMOSTAT

    FDA Adverse Event
    Injury ·VASCULAR SOLUTIONS, INC.·Product code MHW·August 8, 2002

    D/M CRIMP TOOL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·August 14, 2012

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code OYC·April 7, 2021

    GTS ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOEHRINGER MANNHEIM CORP.·Product code CFR·May 2, 1997

    CYPHER DES

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NIQ·February 23, 2006

    ARROW PEDIATRIC MULTI-LUMEN CATHETER SET

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL, INC.·Product code DQO·October 31, 2001

    BRILLANT POST-OP 3-W SILICONE FOLEY,CYL.

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL SDN. BHD.·Product code EZL·August 31, 2020

    D-RAD Self-Tapping Locking Screw intended for the fixation of fractures involving the distal radius. smith&nephew D-RAD 2.4MM X 10MM S-T LOCKING SCREW, REF 74692410, QTY (1), STERILE R

    FDA Enforcement
    Class II ·Terminated·Smith & Nephew, Inc.·April 18, 2018

    D-STAT FLOWABLE HEMOSTAT

    FDA Adverse Event
    Injury ·VASCULAR SOLUTIONS·Product code MHW·March 25, 2005

    BAXTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 15, 1994

    CYPHER DES

    FDA Adverse Event
    Injury ·CORDIS CORP·Product code NIQ·February 14, 2006

    ACCU-CHEK COMFORT CURVE

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS CORP.·Product code CFR·March 10, 2006

    USA SERIES OPERATIVE HYSTEROSCOPE SHEATH

    FDA Adverse Event
    Injury ·GYRUS ACMI, INC.·Product code HIH·November 8, 2012