BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    PENTAX XENON LIGHT SOURCE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Edge™ Diamond FR023-5.5EF Football Round

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172003001·Diamond dental bur, reusable

    Bosworth Re'cord

    FDA UDI
    Harry J Bosworth Company·H66809213151·Polyvinylsiloxane Bite Registration Kit

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471121942·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 125mm

    STRYKER CMF MEDPOR CUSTOMIZED IMPLANT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SURE-LOK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TROCAR WITH HANDLE FOR USE WITH 03.120.014

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code FZX·February 14, 2019

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 6, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    LERADO GLOBAL·Product code IKX·January 17, 2013

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·December 13, 2010