BEUDAMED
    59 results · 68ms · Sources: EU EUDAMED, US FDA

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    TRACTION BOOTS, PAIR

    FDA Adverse Event
    Malfunction ·HOLGER ULLRICH·Product code BWN·December 17, 2021

    TRACTION BOOTS, PAIR

    FDA Adverse Event
    Malfunction ·HOLGER ULLRICH·Product code BWN·May 21, 2021

    INQUIRY¿ STEERABLE EP CATHETER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC·Product code DRF·April 5, 2019

    PROLENE POLYPROPYLENE SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·May 12, 2026

    SILK SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·May 12, 2026

    UNK - CONSTRUCTS: PFNA-II

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·July 15, 2021

    TRACTION BOOTS, PAIR

    FDA Adverse Event
    Malfunction ·HOLGER ULLRICH·Product code FWZ·November 6, 2018

    UNK - PLATES: LOCKING: CALCANEAL PLATE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·May 19, 2021

    UNK - SCREWS: LOCKING: CALCANEAL

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·May 19, 2021

    CELSITE

    FDA Adverse Event
    Malfunction ·B .BRAUN MEDICAL SAS·Product code LJT·April 21, 2017

    FG, FLOWPORT II ADAPTER, STRYKER

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code NBH·July 15, 2020

    ECLIPSE2L BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BALT USA·Product code MJN·February 24, 2022

    HYBRID GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BALT EXTRUSION·Product code MOF·October 12, 2020

    Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use in flexible Endoscopy to provide retraction to assist in tissue resection, exposure, and removal of tissue within the gastrointestinal tract.

    FDA Recall
    Terminated ·Micro-Tech Usa·Product code MND·October 5, 2020

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·June 26, 2018

    CELSITE

    FDA Adverse Event
    Injury ·B.BRAUN MEDICAL SAS·Product code LJT·July 1, 2022

    STELLARIS 23 GAUGE POSTERIOR VITRECTOMY PACK

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQC·July 20, 2012

    ORTHOCORDVIOLET W/MO-6 NDLS PK/12

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code NEW·September 21, 2018

    ORTHOCORDVIOLET W/MO-6 NDLS PK/12

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code NEW·September 21, 2018

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 21, 2022