BEUDAMED
    31 results · 24ms · Sources: EU EUDAMED, US FDA

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    RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053

    FDA 510(k)
    FDA Class 2 ·Neurology

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771012382·K-Wires, Double trocar, .062-inch (1.6mm) diame...

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771048968·K-Wires, Double trocar, .062-inch (1.6mm) diame...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292602·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704912350·

    K-Wire w. double end trocarpoint 1.60mm/229mm, 6 pcs./unit

    FDA UDI
    mahe medical gmbh·EMAHKM711130·K-Wire w. double end trocarpoint 1.60mm...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659484146·K-Wire w. double end trocarpoint _x000D_...

    NA

    FDA UDI
    STERILMED, INC.·10888551018432·ARTHRO-KNIFE BANANA (YELLOW) LEFT, SERRATED

    HYDRAGEL ISO-PAL K20 (PN 3022); HYDRAGEL 7 ISO-PAL (PN 4112); HYDRAGEL 15 ISO-PAL (PN 4132)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IVC THREE BLASTOCYST MEDIUM, CAT # 2007

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

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code JDI·September 11, 2013

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code KWA·September 11, 2013

    CONFIENT

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 27, 2011

    TARGET DEVICE GAMMA3 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·April 22, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·July 10, 2008

    BD TRUCOUNT TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 13, 2021

    BD TRUCOUNT TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code GKZ·July 15, 2021

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code KWA·November 16, 2011

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code JDI·November 16, 2011

    BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·November 30, 2023