BEUDAMED
    8 results · 27ms · 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.

    SPOT-FILM DEVICE 8835

    FDA 510(k)
    FDA Class 2 ·Radiology

    GOODKNIGHT H20, MODEL M-114600-00

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DX-D IMAGING PACKAGE

    FDA 510(k)
    FDA Class 2 ·Radiology

    LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 1, 2022

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 31, 2014

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 12, 2012

    5.0CM SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 12, 2015

    LOGIC TIBIA PS MOD INSRT SZ 3.5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2023