BEUDAMED
    16 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Equinox Advantage

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019

    NIO 5MP, MODEL MDNG-5121

    FDA 510(k)
    FDA Class 2 ·Radiology

    BRIDGEPOINT SPINOUS PROCESS CAMP- POSTERIOR FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLYDESDALE PTC SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019

    ALLOCLASSIC CSF ANCHORAGE CAP 58

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·October 11, 2019

    SULOX, HEAD, S, 32/-3.5, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·October 11, 2019

    OMNIFIT ABC PSL M/S SHELL SIZE 54

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·October 30, 2009

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 17, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 23, 2011

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·September 19, 2008

    UNKNOWN ALLOFIT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·June 7, 2024

    UNKNOWN ALLOCLASSIC SHAFT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·September 16, 2024

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code KMW·May 19, 2024

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019

    DURASUL, ALPHA INSERT, HH/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·March 28, 2018