BEUDAMED
    12 results · 24ms · 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.

    TRIP(TM) NASOGASTRIC SUMP CATHETER

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    Edge™ Diamond ND018-10F Composite Needle

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002578·Diamond dental bur, reusable

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909118252·REVELATION DIAMOND 379-023VF - 5 PACK

    ENDO GIA(TM) STAPLERS, DST SERIES(TM) GIA(TM) STAPLERS, DST SERIES(TM) TA(TM) STAPLERS

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

    RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CAPD DISP DISCONNECT, UV FLASH

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code KDJ·May 23, 2008

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MRU·January 11, 2013

    UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·December 1, 2010

    WHEELCHAIR COMPONENTS

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code KNN·July 3, 2014

    VITEK® 2 AST-GP67 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 31, 2018

    TRI-STAPLE 2.0

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·February 13, 2024

    LIBRE 2 SENSOR FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code QLG·February 9, 2024