BEUDAMED
    1,757 results · 32ms · Sources: EU EUDAMED, US FDA

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    UNK - SCREWS: TRAUMA

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·November 22, 2019

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 15, 2019

    UNK - SCREWS: TRAUMA

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·November 22, 2019

    UNK - NAIL HEAD ELEM: TFNA LAG SCREW

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·November 22, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KXA·November 12, 2019

    BELOTERO BALANCE

    FDA Adverse Event
    Injury ·ANTEIS S.A.·Product code LMH·October 1, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 13, 2019

    UNKNOWN HIP FEMORAL AUGMENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KXA·November 13, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KXA·November 13, 2019

    UNKNOWN HIP ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INT'L LTD. 8010379·Product code KWA·September 6, 2019

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INT'L LTD. 8010379·Product code JDI·September 6, 2019

    SPACEOAR SYSTEM

    FDA Adverse Event
    Injury ·AUGMENIX, INC.·Product code OVB·November 1, 2019

    UNK - NAILS: TFNA

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·November 22, 2019

    Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664

    FDA Enforcement
    Class II ·Terminated·Olympus Corporation of the Americas·July 24, 2019

    OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OER-ELITE.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code FEB·March 25, 2026

    CAMERA "MAJ-554", VIDEO, HEAD, FOR OTV-SC, WITH FILTER

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·December 19, 2025

    SINGLE USE DISTAL COVER MAJ-2315 FOR TJF-Q190V DUODENOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·February 24, 2023

    MAJ-1682 ACCESSORY PORT TUBE WITH SALINE SPIKE - PK 10

    FDA Adverse Event
    Malfunction ·KEYMED (MEDICAL AND INDUSTRIAL EQUIPMENT) LTD.·Product code FEQ·April 23, 2026

    MAJ-1682 ACCESSORY PORT TUBE WITH SALINE SPIKE - PK 10

    FDA Adverse Event
    Malfunction ·KEYMED (MEDICAL AND INDUSTRIAL EQUIPMENT) LTD.·Product code FEQ·May 27, 2026

    MAJ-1682 ACCESSORY PORT TUBE WITH SALINE SPIKE - PK 10

    FDA Adverse Event
    Malfunction ·KEYMED (MEDICAL AND INDUSTRIAL EQUIPMENT) LTD.·Product code FEQ·April 17, 2026