BEUDAMED
    31 results · 22ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO: ECAT LSO PET/CT SCANNER

    FDA 510(k)
    FDA Class 2 ·Radiology

    NATUS MEDICAL

    FDA UDI
    NATUS MEDICAL INCORPORATED·00382830044615·Echo-Screen III Pro Hearing Screening Device TE...

    NorthStar

    FDA UDI
    Seaspine Orthopedics Corporation·10889981214258·Rod-to-Rod Connector, 3.5mm XL

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0315040·Probe, 1.5 inch Ball, Lenke, Straight, Impaction

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0105040·Implant Inserter, 11-13mm, Sleeveless

    NA

    FDA UDI
    aap Implantate AG·04042409071089·APS Plate 135°, 4 holes, L 78

    Flexcera Base Ultra+ Dark Meharry

    FDA UDI
    Envisiontec GmbH·04260683220959·Flexcera Base Ultra+ is a light-curing material...

    RT-PLUS MODULAR CEMENTED KNEE COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BAUMER LOCKING NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Gibralt®

    FDA UDI
    INNO Holdings, Inc.·M711050060135040·Posterior Cervical, Hook, Offset, Right, 3.5mm ...

    Gibralt

    FDA UDI
    Choice Spine, LP·10885862145161·

    NA

    FDA UDI
    aap Implantate AG·04042409071096·APS Plate 135°, 4 holes, L 78

    BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·September 30, 2024

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 20, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 3, 2011

    SENSIA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NVZ·March 10, 2008

    ZENITH® TX2® LOW PROFILE TAA ENDOVASCULAR GRAFT PROXIMAL TAPERED COMPONENT

    FDA Adverse Event
    Death ·WILLIAM COOK EUROPE·Product code MIH·June 16, 2017

    PINNACLE SECTOR II CUP 60MM

    FDA Adverse Event
    Injury ·. DEPUY ORTHOPAEDIC INC, 1818910·Product code KWA·May 25, 2018

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KXA·October 28, 2019

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KXA·October 28, 2019