BEUDAMED
    14 results · 39ms · Sources: EU EUDAMED, US FDA

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    TK Intravascular Administration Set

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074465272·CDH HA COATED MAS 6.5X40

    ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISION FLOW(R) - HELIOX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 22, 2025

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·October 22, 2014

    3002 SECURE II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 1, 2011

    STERRAD 100NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 26, 2013

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 10, 2017

    AZUR VASCULAR PLUG 8

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code KRD·March 29, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022