BEUDAMED
    4,729 results · 50ms · Sources: EU EUDAMED, US FDA

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    Prosthetic Part

    Device
    EU MDR · Eu Md Class 1 ·Ningbo Dacheng Medical Instrument Co., Ltd.·On the market

    Prosthetic Part

    Device
    EU MDR · Eu Md Class 1 ·Ningbo Dacheng Medical Instrument Co., Ltd.·On the market

    Prosthetic Part

    Device
    EU MDR · Eu Md Class 1 ·Ningbo Dacheng Medical Instrument Co., Ltd.·On the market

    Prosthetic Part

    Device
    EU MDR · Eu Md Class 1 ·Ningbo Dacheng Medical Instrument Co., Ltd.·On the market

    Prosthetic Part

    Device
    EU MDR · Eu Md Class 1 ·Ningbo Dacheng Medical Instrument Co., Ltd.·On the market

    Prosthetic Part

    Device
    EU MDR · Eu Md Class 1 ·Ningbo Dacheng Medical Instrument Co., Ltd.·On the market

    UNKNOWN KNEE COMPONENT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·April 28, 2005

    ARROW

    FDA Adverse Event
    Malfunction ·FH INDUSTRIE·Product code KWT·March 23, 2022

    ELEMENT IMPLANT, PF 4,5, E 4,2, L 11,0

    FDA Adverse Event
    Injury ·THOMMEN MEDICAL AG·Product code DZE·October 6, 2018

    CERTAIN GOLD-TITE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code NHA·May 29, 2026

    SRS SHOULDER GLENOSPHERE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code PHX·July 2, 2025

    SRS SHOULDER GLENOSPHERE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code PHX·July 2, 2025

    28MM +16 V40 TAPER VIT HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code KWY·August 14, 2009

    prosthetic parts

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Ge Rui Hong Kang Medical Technology(SanHe) Co.,Ltd·140 devices

    Prosthetic Part

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Ningbo Dacheng Medical Instrument Co., Ltd.·6 devices

    PROSTHETIC PARTS

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Shijiazhuang Perfect Prosthetic Manufacture Co.,Ltd·1 device

    AXIOM REG IMPLANT

    FDA Adverse Event
    Malfunction ·ANTHOGYR·Product code DZE·January 19, 2018

    ONYX IMPLANT

    FDA Adverse Event
    Malfunction ·NORIS MEDICAL LTD·Product code DZE·October 4, 2023

    ONYX IMPLANT

    FDA Adverse Event
    Malfunction ·NORIS MEDICAL LTD·Product code DZE·October 4, 2023

    ONYX IMPLANT

    FDA Adverse Event
    Malfunction ·NORIS MEDICAL LTD·Product code DZE·October 4, 2023