BEUDAMED
    24 results · 30ms · Sources: EU EUDAMED, US FDA

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    MEDTRONIC ARES ANTIBIOTIC-IMPREGNATED CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169601383·SPACER 2110560 OLIF25 20MM 0 DEG 16X60

    PHASER PHO75 LW (1 dwt)

    FDA UDI
    ARGEN CORPORATION, THE·D818110560·Gold based noble metal

    LuxaBite

    FDA UDI
    DMG Chemisch-Pharmazeutische Fabrik GmbH·EDMG1105600·Bite registration material automix system. The ...

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317320728·

    Wedge 15 CF ExaFix™

    FDA UDI
    MACROMEDICS B.V.·08719425700960·Carbon fiber wedge, fit for ExaFix,15 degrees

    Luneray

    FDA UDI
    Nucletron B.V.·08717213022768·Catheter 6F 50cm, needle 37mm R30mm

    Luneray

    FDA UDI
    Nucletron B.V.·08717213054059·Catheter 6F 50cm, needle 37mm R30mm

    EASY TALK BLOOD GLUCOSE MONITORING SYSTEM MODEL: 6277

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PORTRAIT FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·July 27, 2020

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 13, 2014

    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

    LCS COMPLETE M/B PAT POR STD+

    FDA Adverse Event
    Injury ·9616671 DEPUY IRELAND·Product code NJL·May 14, 2013

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·September 23, 2014

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 1, 2011

    UNKNOWN LUMBAR IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022

    ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020