BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    CLIQ DV-300 ASPIRATOR

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517565303·CoRoent Ant TLIF PEEK, 13x12x30mm 8°

    AGXO

    FDA UDI
    Oticon A/S·05707131258113·H150, MINIBTE 312 WL 85 TC AGXO

    Aileron Expandable Posterior Fusion System

    FDA UDI
    Life Spine, Inc.·00190837000028·

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857560680·Trial With Stop Size 12x14x11 mm, 4 Degrees

    Aileron Expandable Posterior Fusion System

    FDA UDI
    Life Spine, Inc.·00190837000011·

    Aileron Posterior Fusion System

    FDA UDI
    Life Spine, Inc.·00190837043995·Aileron Implant Plate, Small, Thin Foot

    SIMPLELINE II MODEL SOFX483408R, SOFX483410R TOTAL 44 MODELS

    FDA 510(k)
    FDA Class 2 ·Dental

    BLOOD PRESSURE MONITOR, MODEL M100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON BALLAST SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·December 9, 2019

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FPA·December 8, 2023

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014

    HI-TORQUE FLOPPY II GUIDE WIRE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code DQX·May 29, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 13, 2011