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

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    NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POWDER FREE NITRILE PATIENT EXAMINATION GLOVE, BLUE COLORED AND WHITE (NON-COLORED). NON-STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TSRH(R) SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    1.5MM DRILL BIT/MINI QC/65MM

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTW·May 9, 2014

    1.5MM DRILL BIT/MINI QC/65MM

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HWE·May 9, 2014

    INFERIOR TURBINATE BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC·Product code EQJ·July 27, 2011

    RACK Ø6.5/7.3

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FSM·June 21, 2013

    CD HORIZON AGILE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC ORTHOPEDIC INC.·Product code NQP·September 18, 2008

    INTRAUTERINE ACCESS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LKF·December 10, 2020

    CANTATA 2.9 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·September 14, 2017

    SELECTIVE SALPINGOGRAPHY CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LKF·November 19, 2021