BEUDAMED
    23 results · 21ms · Sources: EU EUDAMED, US FDA

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    SHARPS CONTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017729·K-Wire, Double Ended, Trocar Point, Diameter Si...

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902096044·HOLDER 9110262 IMPLANT TPRD 14/23MM

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·50885380030480·10cc Secure Tube

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306815720·Richardson-Eastman Retractor, Double Ended, Lar...

    Utrecht Interstitial Fletcher CT/MR Applicator

    FDA UDI
    Nucletron B.V.·08717213034822·Interstitial Ovoid (right) 30mm 25°, R10

    Xhibit

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522131141·DISPLAY,21.5",CAPACITIVE TOUCH,BLACK,ANTI-GLARE

    FLEXI-LITE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG

    FDA 510(k)
    FDA Unclassified ·Unknown

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 5, 2023

    TELAMON FUSION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·August 5, 2016

    TELAMON® FUSION DEVICE

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·August 3, 2012

    TELAMON® FUSION DEVICE

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·August 3, 2012

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 13, 2013

    PROLONG BLOCK BEVEL - 19 GA X 50MM

    FDA Adverse Event
    Malfunction ·I-FLOW, LLC·Product code CAZ·September 11, 2014

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·May 20, 2011

    Comprehensive HHR Tess Cleat, Item Nos. 110260 110261 110262 110263 Product Usage: N/A

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code NA·August 21, 2019

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC·Product code GJS·July 14, 2017

    SS 3.5Mm Pellet Insertion Tray with large Gloves Catalog Number: B1352R1

    FDA Enforcement
    Class II ·Terminated·Busse Hospital Disposables, Inc.·June 8, 2022

    Comprehensive HHR Tess Cleat, Item Nos. 110260 110261 110262 110263 Product Usage: N/A

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019