BEUDAMED
    149 results · 23ms · Sources: EU EUDAMED, US FDA

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    METANEB

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 32mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665033595·

    Diversatek Healthcare

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·M7831240320·Straight Thoracic Catheter, 32 French x 20 IN

    MECHANICAL WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ATTAIN 6216A-MP MULTI-PURPOSE GUIDE CATHETER FOR LEFT-HEART DELIVERY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HPS TIBIAL LINER #4 H10

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A·Product code JWH·July 5, 2023

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 15, 2013

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 27, 2014

    RADIAL JAW 4 BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·June 14, 2011

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·June 22, 2018

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Injury ·COOK INC·Product code GEX·March 29, 2016

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Injury ·COOK INC·Product code GEX·August 29, 2016

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·October 3, 2017

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·August 7, 2017

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Injury ·COOK INC·Product code GEX·December 13, 2017

    CN LOCK SCREW, F THREAD, Ø4.0MM X 40MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·November 26, 2024

    CORTICAL BONE SCREW, Ø3.5MM X 28MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code KTW·November 27, 2024

    TIGERTAPE CERCLAGE W/O NEEDLE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·November 27, 2024

    CORTICAL BONE SCREW, Ø3.5MM X 26MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·November 26, 2024

    CN LOCK SCREW, F THREAD, Ø4.0MM X 36MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·November 26, 2024