BEUDAMED
    10 results · 20ms · 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 ×

    Titan

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Oticon

    FDA UDI
    Oticon A/S·05707131286291·NERA2 PRO TI, MINIRITE 312 WL CNB

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100028·BLUMENTHAL SPECULUM X-HEAVY

    REZUM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·April 23, 2024

    Tibial Cutting Block Slide Assembly

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215041366·

    IFS PROFILE PLATES, SCREWS, AND WASHERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BRENNEN MEDICAL SILVER GLUCAN WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    ALIGN URETHRAL SUPPORT SYSTEM RETROPUBIC

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED·Product code OTN·May 31, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    UNKNOWN ZIMMER HIP

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JDI·August 29, 2008