BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Prevena Plus Incision Management System, Prevena Plus Duo Incision Management System

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

    PREVENA PLUS INCISION MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC·Product code OMP·September 24, 2021

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158118·Lateral Implant, 18mm x 8mm x 55mm, 10 Deg

    Regatta

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158101·Lateral Implant, 18mm x 8mm x 55mm, 0 Deg

    INTELLISPACE ECG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    STERRAD 200 STERILIZATION SYSTEM

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 20, 2013

    OT VERIO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 27, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 17, 2014

    CD HORIZON SPINAL SYSTEM

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