BEUDAMED
    154 results · 25ms · Sources: EU EUDAMED, US FDA

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    DilaCheck Nitrile Powder Free Examination Glove, (Sterile)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Back-n-Shape II

    FDA UDI
    MEDICAL SPECIALTIES INCORPORATED·00802357630356·

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017811·K-Wire, Double Ended, Trocar Point, Diameter Si...

    Valencia Pedicle Screw System

    FDA UDI
    Altus Spine, LLC·00843210109534·Small, 30mm-35mm Cross Connector Assembly

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613084837·K-Wire, Double Ended, Trocar Point, Diameter 0....

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017828·K-Wire, Double Ended, Trocar Point, Diameter 0....

    SMARTPILOT VIEW MODEL MK04500

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SLEUTH IMPLANTABLE ECG MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Free-Lock®

    FDA UDI
    Zimmer, Inc.·00889024034471·

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 10, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS, INC.·Product code KWP·June 11, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·July 15, 2011

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·December 21, 2018

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·May 29, 2019

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019

    1030489-2019-01511

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019

    ULTRATHANE MAC-LOC LOCKING LOOP MULTIPURPOSE DRAINAGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code FGE·December 13, 2024

    1030489-2019-01423

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NDN·December 13, 2019

    ULTRATHANE MAC-LOC LOCKING LOOP MULTIPURPOSE DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FGE·October 24, 2024