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

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    VOCSN Unified Respiratory System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LANDANGER

    FDA UDI
    LANDANGER·03661219432623·

    COMEN MULTI-PARAMETER PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2025

    DBX PUTTY, 5CC

    FDA Adverse Event
    Injury ·MUSCULOSKELETAL TRANSPLANT FOUNDATION·Product code MQV·October 8, 2014

    6000 CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    VOYAGER NC CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·July 15, 2011

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2024

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 4, 2025

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 13, 2025

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·June 20, 2025