BEUDAMED
    11 results · 19ms · 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.

    MODIFIED MODEL 2001 FIBER OPTICS CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACETABULAR SCREW RING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTERIOVENOUS BLOOD TUBING SET FOR

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

    URIC ACID REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code KNK·April 15, 2011

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    FORCETRIAD ENERGY PLATFORM

    FDA Adverse Event
    Injury ·COVIDIEN LP·Product code GEI·June 11, 2014

    ASP AUTOMATIC ENDOSCOPE REPROCESSOR WITH PRINTER

    FDA Adverse Event
    Injury ·MINNTECH CORPORATION·Product code KOG·October 27, 2010

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·November 15, 2012