BEUDAMED
    19 results · 23ms · 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 ×

    SYNGO, CT CARDIAC FUNCTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197042482·CERA-CUT® Gorney Facelift Scissors geboge...

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011123585000·Super hard metal burs, with cross toothing cut,...

    BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP

    FDA 510(k)
    FDA Class 2 ·Dental

    FLOSTAR NEEDLELESS CONNECTOR, MODEL FS3000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·May 18, 2026

    KANGAROO

    FDA Adverse Event
    Injury ·CARDINAL HEALTH 200, LLC·Product code KNT·April 6, 2026

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·April 17, 2026

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·May 1, 2026

    BACTISEAL VENTRICULAR CATHETER

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·August 22, 2023

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·October 16, 2024

    GEM PREMIER 4000

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code CHL·June 10, 2011

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·May 17, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    G7 NEUTRAL E1 LINER 36MM D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·March 23, 2023

    36MM COCR MOD HD STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 23, 2023

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·February 5, 2026

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·December 30, 2024

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·November 25, 2025