BEUDAMED
    9 results · 22ms · 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.

    EQUINOXE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MM-CE 11 (BEHIND THE EAR)

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    LASER FLARE CELL METER FC-1000

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CER BIOLOXD OPTION HD 32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 29, 2025

    CER BIOLOXD OPTION HD 32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 29, 2025

    CER BIOLOXD OPTION HD 32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 29, 2025

    APPLICATOR INNER SHAFT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code LXH·February 27, 2013

    UNICEL® DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·February 7, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

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