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

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    SMART LABEL, PROPOFOL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Equator

    FDA UDI
    Preat Corporation·00842092182321·Equator Abutment for Straumann BLX RB x 8mm

    LRT ATTACHMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    CONTROL PLASMA N, PROC CONTROL PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·April 18, 2016

    BMT GB KNEE STM 12X40

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OIY·June 1, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 5, 2025

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 5, 2014

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·June 20, 2011

    11MM TI CANNULATED FEMORAL NAIL 400MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDN·June 3, 2013

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·April 18, 2016