BEUDAMED
    28 results · 30ms · Sources: EU EUDAMED, US FDA

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    SPECTRUM SPINE SPINOUS PROCESS DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GYRUS ACMI, INC

    FDA UDI
    Gyrus ACMI, LLC·00821925011656·TABB KNIFE EBONY FINISH

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694033596·1.6mm 6 Hole L Plate, Right

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776143923·24Fr Obturator

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00840326401965·Carbide Bur Pointed

    NA

    FDA UDI
    STRYKER CORPORATION·07613153094548·3.2mm Cross Cut Fissure

    CAL/RAD MARK VI/VDC-505 DOSE CALIBRATOR, MODEL 34-165

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·May 24, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 30, 2014

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·July 26, 2024

    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·October 6, 2022

    DENALI JUGULAR SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 27, 2023

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·July 13, 2020

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·July 15, 2020

    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·February 9, 2023

    DENALI JUGULAR SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·November 21, 2023

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 10, 2023

    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·December 6, 2024