BEUDAMED
    233 results · 19ms · Sources: EU EUDAMED, US FDA

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    MILLER-GALANTE TOTAL KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KRQ·August 24, 1992

    FINN SEGMENTAL FEMORAL

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code KRQ·April 30, 2002

    LT TOTAL KNEE PROSTHESIS

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code KRQ·April 30, 2002

    Short tibial bearing MK4 - Std, STM, Catalog No. SMMLTB02. Knee prosthesis component.

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code KRQ·August 24, 2022

    Prosthesis, Knee, Patello/Femorotibial, Constrained, Cemented, Polymer/Metal/Polymer

    FDA classification
    FDA Class 2 ·Prosthesis, Knee, Patello/Femorotibial, Constrained, Cemented, Polymer/Metal/Polymer

    HU-FRIEDY

    FDA UDI
    HU-FRIEDY MFG. CO., LLC·10889950045043·Univ of ACTA Cheek Retractor

    HU-FRIEDY

    FDA UDI
    HU-FRIEDY MFG. CO., LLC·10889950014667·Paquette Palatal Knife

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007450·Cala kIQ Band, Large

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007412·Stimulator

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007474·Cala kIQ Band, Large

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007429·Base Station

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007498·Cala kIQ Band, Small

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007481·Cala kIQ Band, Medium

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007436·Cala kIQ Band, Small

    Cala kIQ

    FDA UDI
    CALA HEALTH, INC.·00851749007443·Cala kIQ Band, Medium

    Cala kIQ

    FDA 510(k)
    FDA Class 2 ·Neurology

    Cala kIQ

    FDA 510(k)
    FDA Class 2 ·Neurology

    Cala kIQ

    FDA 510(k)
    FDA Class 2 ·Neurology

    Cala kIQ Plus

    FDA 510(k)
    FDA Class 2 ·Neurology

    MedSource Bags

    FDA UDI
    MEDSOURCE INTERNATIONAL LLC·00840155407053·Basic Life Support Bag