BEUDAMED
    21 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    DYNANAIL ANKLE ARTHRODESIS NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BILI-THERAPY SPOT TYPE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GLOVCO EBONY

    FDA 510(k)
    FDA Class 1 ·General Hospital

    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

    AGX

    FDA UDI
    Widex A/S·05706069750409·Audigy AGXWD-FS (Winter silver S-330 ) Telecoil...

    ASTRON CLEAR SPLINTS

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

    PROSOUND F75 ULTRASOUND SCANNER

    FDA Adverse Event
    Malfunction ·HITACHI ALOKA MEDICAL, LTD·Product code GXX·July 16, 2014

    CUS AG X WIDENED TALAR SIZE 6

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code HSN·May 15, 2013

    ACCLAIM ENCORE 2.25

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·September 17, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·May 17, 2011

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 2, 2020

    R3 XLPE INSERT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDI·May 25, 2025