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

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    LDR Spine ROI-C Cervical Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROI-C IMPLANT, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·LDR MÉDICAL·Product code OVE·September 21, 2021

    AGXO

    FDA UDI
    Oticon A/S·05707131282057·H150V2, MINIBTE 312 WL 85 CBE AGXO

    PEEK Temporary Abutment

    FDA UDI
    BICON, LLC·00813110027894·5.0 x 6.5mm PEEK Temporary Abutment - 2.0mm Post

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962161975·WEISMAN PEDERSON, LEFT SIDE OPENING, LARGE

    FIXPINE II SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LANO-E POWDER-FREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 6, 2013

    36X11 CRESCENT CAGE

    FDA Adverse Event
    Other ·MEDTRONIC SOFMAR DANEK·Product code MAX·June 30, 2011

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·September 3, 2008

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code DQY·December 25, 2016

    VENATECH CONVERTIBLE

    FDA Adverse Event
    Malfunction ·B.BRAUN MEDICAL SAS·Product code DTK·January 5, 2018

    METACROSS RX PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·October 15, 2019