BEUDAMED
    12 results · 22ms · 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 ×

    BASKET LITTER CARRIER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    THORACIC ANTERIOR SPINAL FIXATION PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SLEEPTRACE 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 12, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 6, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·January 15, 2013

    REGENEREX ACETABULAR SHELL 64ODX54ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 6, 2018

    36MM COCR BIOMET FEM HD -3 NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 23, 2018

    HWAL ARCOMXL ALLPOLY 36IDX54OD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 6, 2018

    ARCOS HA MODULAR REVISION CONE PROXIMAL BODY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 6, 2018

    36MM COCR BIOMET FEM HD -3 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDG·August 27, 2018

    ARCOS STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·August 6, 2018