BEUDAMED
    37 results · 31ms · Sources: EU EUDAMED, US FDA

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    3D MANUAL COARSE MANIPULATOR MN-188NE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Essential Kit

    FDA UDI
    MEDIVATORS INC.·40677964010765·Essentials Kit includes Intercept Bedside Kit, ...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001130·artVeneer life lower anteriors, UIM, A35

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031189·PrimaLOK FF 30mm Implant Assembly

    primaLOK FF

    FDA UDI
    Wenzel Spine, Inc.·00813210021969·primaLOK FF 30mm Implant Assembly, Sterile ...

    CURE LP

    FDA UDI
    MEDITECH SPINE, LLC·B167900011300·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031844·PrimaLOK FF 30mm Implant Assembly, Sterile

    CURE LP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1900011300·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031899·PrimaLOK FF 30mm Implant Assembly, 2 Pack, Sterile

    RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HARDYDISK, NALIDIXIC ACID, 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·January 15, 2014

    STD BRL 4-HOLE PLATE 135 DEG

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JDO·October 10, 2018

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 26, 2013