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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    APLIO ARTIDA V2.0 SSH-880CV

    FDA 510(k)
    FDA Class 2 ·Radiology

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099709·MX MLR BDS R/L SE ASIA ASST100

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036027384·

    VEINLASE, MODEL E50-K8-B5, SPECTRUM K8, MODEL E50-K8-B9

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    THROMBOMAX-HS WITH CALCIUM, MODEL T6540

    FDA 510(k)
    FDA Class 2 ·Hematology

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2024

    VCL CT BRD UD 36IN 0 S/A CTX

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·October 28, 2019

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 2, 2013

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 15, 2014

    PLEUR-EVAC CHEST DRAINAGE SYSTEM, DRY SUCTION

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code KDQ·April 11, 2011