BEUDAMED
    35 results · 29ms · Sources: EU EUDAMED, US FDA

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    LnK Cervical Interbody Fusion Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100547·LIEBERMAN SPECULUM SOLID SMALL

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837106423·Static Expandable Cage Trial, 10mm x 28mm x 6mm...

    OPTIGEN ALLERGEN SPECIFIC IGE ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    HOSPIRA INFUSION BLOOD SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 30, 2013

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·September 12, 2013

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code BRZ·September 13, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 17, 2013

    NDEHP Y-BLOOD SET W/FILTER PUMP 203CM

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 24, 2011

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 10, 2013

    DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·June 7, 2013

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 6, 2011

    THERMOTEX

    FDA Adverse Event
    Injury ·THERMOTEX THERAPY SYSTEM LTD.·Product code IRT·September 4, 2008

    SOLUSET 100X60

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 22, 2013

    SOLUSET 100X60

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 22, 2013

    KRD DEVICE, EMBOLIZATION, VASCULAR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 19, 2019

    SECONDARY SET CAIR CLAMP NON-DEHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·May 5, 2014