BEUDAMED
    324 results · 73ms · Sources: EU EUDAMED, US FDA

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    CURAD SIZE D COMPRESSION STOCKINGS

    FDA Adverse Event
    UNK·Product code FQL·January 7, 2019

    VNUS CLOSURE

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·November 18, 2025

    JOBST RELIEF -MEDICAL LEGWEAR-

    FDA Adverse Event
    Malfunction ·BEIERSDORF-JOBST, INC·Product code DWL·May 12, 2002

    JOBST MEDICAL COMPRESSION STOCKING 15-20 MMHG SIZE MEDIUM CAT NO. 119179, BLACK

    FDA Adverse Event
    Injury ·BSN MEDICAL, INC.·Product code LLK·August 9, 2018

    SCD COMFORT KNEE LENGTH MED

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code JOW·June 23, 2022

    Truform Therapeutic Classic Medical Style Compression Stockings 20-30 mmHG, Truform Therapeutic Classic Medical Style Compression Stockings 30-40 mmHG, A Div of SAI, Cincinnati, OH 45209 Product Usage: To help relieve tired, heavy legs, and moderate to pronounced varicose veins and swelling.

    FDA Recall
    Terminated ·Surgical Appliance Industries·Product code FQL·October 7, 2011

    ACTIVECARE

    FDA Adverse Event
    MEDICAL COMPRESSION SYSTEMS LTD.·Product code JOW·September 30, 2011

    ACCESSORY PACK MODEL 502

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·February 15, 2022

    COMFORT WEAR

    FDA Adverse Event
    Death ·THE MARENA GROUP, INC.·Product code MDR·March 26, 2003

    3728LF TED STKG NYL T/L LR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code FQL·February 26, 2015

    TRITANIUM BPLATE TRIATHLON S5

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·December 28, 2018

    TRIATHLON CR FEM COMP #4 R-CEM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·December 21, 2018

    HYALGAN

    FDA Adverse Event
    Injury ·FIDIA SPA·Product code MOZ·August 12, 2009

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GEI·March 26, 2021

    EVLT KITS

    FDA Adverse Event
    Other ·DIOMED, LTD.·Product code GEX·September 4, 2007

    SCD DEVICE - SEQUEL SYSTEM

    FDA Adverse Event
    Injury ·KENDALL VASCULAR THERAPY·Product code JOW·June 30, 1999

    KENDALL SCD

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG PLAINFIELD·Product code JOW·January 24, 2018

    TRABECULAR METAL REVERSE SHOULDER SYSTEM INSTRUMENTATION BAS

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LXH·May 11, 2007

    MAXGUARD EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·January 14, 2016

    3856LF TED STKG NYL T/L LL

    FDA Adverse Event
    Malfunction ·COSTA RICA·Product code FQL·October 21, 2014