BEUDAMED
    33 results · 25ms · Sources: EU EUDAMED, US FDA

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    Honorst Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM

    Conventional Lead Apron .5mm Xtra Large 25 X 40

    FDA UDI
    Flow X Ray Corporation·00843696123734·Conventional Lead Apron .5mm Xtra Large 25 X 40...

    SprintRay High Impact Denture Base - Original Pink

    FDA UDI
    Sprintray, Inc.·00850039704192·SprintRay High Impact Denture Base is a light-c...

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112649·BARRON CORNEAL PUNCH 8.25MM

    ECAT PET SCANNER, MODELS ECAT EXACT AND ECAT EXACT HR+ AND ECAT ART

    FDA 510(k)
    FDA Class 2 ·Radiology

    P pro Crown & Bridge

    FDA 510(k)
    FDA Class 2 ·Dental

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·June 21, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 5, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·April 12, 2023

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·August 5, 2015

    WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·October 13, 2021

    EON MINI

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 21, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    STANDARD MODEL BED FL19F-1

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FMS·July 2, 2013

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·November 30, 2020

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·November 30, 2020

    ARCHITECT CA 19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·August 31, 2020

    LOTUS VALVE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NPT·May 12, 2021

    HEARTWARE VENTRICULAR ASSIST SYSTEM - OUTFLOW GRAFT

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·June 5, 2020