BEUDAMED
    11 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 ×

    ManipulatOR PRO, ManipulatOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100165·KRATZ-BARRAQUER SPECULUM SMALL

    ADVANCED TURBO DRIVE SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PHILIPS UVA (/09) AND PHILIPS UVA-1 (/10) ULTRAVIOLET LAMPS

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

    SURGICEL ABSORBABLE HEMOSTAT UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code LMG·October 12, 2021

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·October 12, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 12, 2025

    ENDOPATH XCEL BLUNT TIP TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·June 6, 2013

    RELIANCE CM CEMENTED HIP #3

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code JDI·June 23, 2011

    NA

    FDA Adverse Event
    Injury ·ASCENT HEALTHCARE SOLUTIONS·Product code NLQ·September 4, 2008

    VENTED AUTOFEED CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 25, 2016