BEUDAMED
    10 results · 18ms · 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.

    JP-2 RESPIRATORY MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DD cube ONE ML

    FDA UDI
    Dental Direkt GmbH·EDDIG8320051·DD cube ONE® ML are dental mill blanks made fro...

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153547·

    MEDTRONIC MINIMED PARADIGM RESERVOIR, MODEL MMT-332

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RETROGRADE FEMORAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KARL STORZ

    FDA Adverse Event
    Injury ·KARL STORZ ENDOSCOPY·Product code KQT·January 21, 2004

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·March 7, 2014

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·November 14, 2012

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 13, 2010

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021