BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    HEADLOC CERAMIC HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623812·PEEK Corp Core, Ø14x26mm

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902997693·INSTRUMENT 6971426 RAIL PUNCH 6MMX12MM

    MP2, X2, MP5, MP20, MP30, MP40, MP50, MP60, MP70, MP80, AND MP90 INTELLIVUE PATIENT MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    da Vinci Xi 8mm Endoscope, 0 degree, da Vinci Xi 8mm Endoscope, 30 degree

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

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·December 12, 2019

    EON

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 4, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·January 13, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 31, 2014

    ACTTIVE ARTICULATION HIP SYSTEM - DUAL MOBILITY BEARING E1 ANTIOXIDANT INFUSED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 7, 2019

    G7 OSSEOTI 3 HOLE SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 7, 2019