BEUDAMED
    27 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Aquilion Exceed LB

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    Synthes GmbH·10886982151629·2.4MM CANNULATED SCREW LONG THREAD 28MM

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF2118280·2.4mm Cannulated Screw, Long Thread, 28mm

    Diamond Orthopedic, LLC

    FDA UDI
    DIAMOND ORTHOPEDIC, LLC·B551DMD2118280·2.4mm, Cannulated Screw, Long Thd., 28mm

    CYNOSURE ACCLAIM DERMATOLOGY LASER

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

    CLEARSPLINT ES

    FDA 510(k)
    FDA Unclassified ·Unknown

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

    GELB MOUTHGUARD

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·April 10, 2019

    ASTRON CLEAR SPRINT

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 14, 2020

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 17, 2019

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 16, 2019

    ASTRON CLEAR SPLINT

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 22, 2020

    ASTRON CLEAR SPLINT LOWER

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 30, 2020

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·May 4, 2020

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·September 6, 2019

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·HEARTWARE·Product code DSQ·October 29, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 10, 2011

    LINOX SMART SD 60/16

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVY·July 8, 2013