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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SILICONT BUR BLOCK

    FDA 510(k)
    FDA Class 1 ·Dental

    Bosworth Fastray LC

    FDA UDI
    Harry J Bosworth Company·H66809214061·Fastray LC Standard Kit Pink

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150584·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 150mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123793·K-WIRE - DOUBLE TROCAR 1.4mm DIA x 150mm

    ARTERIAL BLOOD SAMPLING KIT

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    INCLUSIVE TAPERED IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    INCLUSIVE TAPERED IMPLANT

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 17, 2018

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·January 17, 2013

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    STYKE-FLOW2

    FDA Adverse Event
    STRYKER ENDOSCOPY DIV. OF STRYKER CORP·Product code GCX·July 2, 2014