BEUDAMED
    18 results · 29ms · Sources: EU EUDAMED, US FDA

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    Wright Jones Fracture System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304270503·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528128220·3.0 X 26mm Cannulated Headed Screw, T10

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A18302680·18mm H x 30mm W x 26mm L x 8 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A183026150·18mm H x 30mm W x 26mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A183026120·18mm H x 30mm W x 26mm L x 12 degrees ALIF

    MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S5 - LATER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·December 16, 2020

    DASH Flex 12 Centrifuge, LabCorp

    FDA UDI
    DRUCKER DIAGNOSTICS·00810052860206·General purpose laboratory centrifuge for sampl...

    CLYDESDALE SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECTRO SENSOR -BODY COMPOSITION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MOTO PARTIAL KNEE TIBIAL INSERT FIX S4 LM - 8MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·October 26, 2023

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    TRUFIT

    FDA Adverse Event
    Malfunction ·MANSFIELD MANUFACTURING SITE·Product code MQV·June 21, 2013

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MAX·December 18, 2019

    DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·August 13, 2021

    DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·July 27, 2022

    COONS DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·July 28, 2022