BEUDAMED
    13 results · 21ms · 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.

    SIGMA DIAGNOSTICS ACCUCLOT CONTROL III

    FDA 510(k)
    FDA Class 2 ·Hematology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517403513·CoRoent® XL, 12x18x55mm 10°

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981255·anteriors; shade C1; mould BIM2

    Symmetry Surgical®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482087268·Symmetry® Grasper, Murray, Ratcheting Handle, 5 mm

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024160729·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024160736·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024160712·

    SCRAMBLER ST 5 TENS DEVICE

    FDA 510(k)
    FDA Class 2 ·Neurology

    PRODENSE Bone Graft Substitute

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 20, 2014

    VITROS CHEMISTRY PRODUCTS PHBR SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code DLZ·February 27, 2013

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 1, 2011

    L.C. 5000/CE 2-CHANNEL PUMP (50/CASE)

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 22, 2013