BEUDAMED
    11 results · 29ms · 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 ×

    Maestro Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837073732·Walker Connector

    ENDOSCOPIC CLIP SYSTEM

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

    ZODIAC DYNAMO SEMI-RIGID SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Widex

    FDA UDI
    Widex A/S·05706069792744·Widex UNIQUE U-PA (Tan silk ) 30, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069819441·Widex UNIQUE U-FS (Tan silk ) 30, Telecoil, RC ...

    ALINITY S HBSAG REAGENT KIT

    FDA Adverse Event
    Injury ·ABBOTT IRELAND·Product code QHM·October 4, 2022

    PLUMA+ UK WITH 3PIN

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 11, 2013

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 15, 2011

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORTION·Product code LGW·September 23, 2008

    ALINITY S HBSAG REAGENT KIT

    FDA Adverse Event
    Injury ·ABBOTT IRELAND·Product code QHM·November 29, 2022