BEUDAMED
    34 results · 25ms · 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 ×

    Change Healthcare Enterprise Viewer

    FDA 510(k)
    FDA Class 2 ·Radiology

    MOBLVAC W.C.

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

    NUCLEIC ACID DETECTION IMMUNOASSAY (NADIA) PSA ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    UNKSAVVY

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code LIT·February 18, 2019

    UNKSAVVY

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code LIT·February 19, 2019

    BRAVO

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code FFT·June 19, 2008

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 21, 2013

    CLARION

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·July 19, 2011

    PERCUFLEX PLUS URETERAL STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code FGE·September 30, 2008

    REVEAL LINQ

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DSI·September 30, 2020

    THE Q-TRAK SUBCUTANEOUS ELECTRODE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 25, 2025

    SQ-RX PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 25, 2025

    THE Q-TRAK SUBCUTANEOUS ELECTRODE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 24, 2025

    SQ-RX PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 24, 2025

    SQ-RX PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 24, 2025

    SQ-RX PULSE GENERATOR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 24, 2025

    THE Q-TRAK SUBCUTANEOUS ELECTRODE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 24, 2025

    THE Q-TRAK SUBCUTANEOUS ELECTRODE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 25, 2025

    SQ-RX PULSE GENERATOR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 23, 2025

    THE Q-TRAK SUBCUTANEOUS ELECTRODE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 23, 2025