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

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    SIGNA Pioneer

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517637635·CoRoent Ant TLIF PEEK, 14x13x34mm 15°

    UNIVERSAL RECONSTRUCTION RIBBON

    FDA UDI
    Biomet Orthopedics, LLC·00887868004285·

    ATRAMAT

    FDA UDI
    Internacional Farmacéutica, S.A. de C.V.·07500142063756·ATRAMAT SILK SURGICAL SUTURE BLACK USP 3-0 EP 2...

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013401876·SINGLE INSTRUMENT

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·10840200301876·SINGLE INSTRUMENT

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code LXH·February 10, 2020

    BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES (BT-V2S)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DIGITAL FLAT PANEL X-RAY DETECTOR / 1012WCA

    FDA 510(k)
    FDA Class 2 ·Radiology

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·September 27, 2018

    CD HORIZON SOLERA VOYAGER SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·November 12, 2018

    CD HORIZON SOLERA SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·December 13, 2019

    CD HORIZON SOLERA SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·December 13, 2019

    CD HORIZON SOLERA SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·August 16, 2019

    4.5MM LCP® CONDYLAR PLATE 6 HOLES/170MM-LEFT

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HRS·June 3, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 29, 2011

    MARYLAND JAW LAP (37CM)

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·October 6, 2014

    CD HORIZON SOLERA SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·September 18, 2019

    CD HORIZON SOLERA SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·March 25, 2019

    CD HORIZON SOLERA SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·May 9, 2018