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

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    PROTEXIS LATEX BLUE WITH NEU-THERA POWDER-FREE SURGICAL GLOVES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Flexitron

    FDA UDI
    Nucletron B.V.·08717213027183·Flexitron Transfer Tube for 4F Flexibles (26)

    GE LOGIQ P5 MODEL H44662LD

    FDA 510(k)
    FDA Class 2 ·Radiology

    EMIT (R) TOX SALICYLIC ASSAY, MODEL 7SO19UL, EMIT (R) TOX SALICYLIC ACID CALIBRATORS, MODEL 7S109UL

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    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

    VIDEO TELESCOPE "ENDOEYE HD II", 10 MM, 30°, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·January 15, 2026

    ASTRON CLEAR SPLINTS

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 8, 2025

    ATTUNE RP TIB BASE SZ 7 CEM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code NJL·October 24, 2019

    AUTOLUBE-III

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEI·May 7, 2013

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·June 2, 2011

    ROTALINK CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code MCX·August 12, 2008