BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    TUBE-STRAP

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Wagner SL Revision Stem Lateral and Wagner Cone Prosthesis System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GUIDED MEDICAL POSITIONING SYSTEM (GMPS)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 6, 2014

    UNKNOWN EXTERNAL NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·October 15, 2012

    UNKNOWN PRODUCT - LOCKING SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·August 4, 2010

    NEURO SPG-1X1"-STERILE- 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 20, 2025

    NEURO SPNG-1/2X3"-STRL- 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 7, 2025