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

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    Senographe Pristina

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517638540·CoRoent Ant TLIF PEEK, 16x13x30mm 12°

    Mouthpiece, Disposable, 1.01 OD, 2.625" L

    FDA UDI
    A-M SYSTEMS, LLC·00817081023954·Mouthpiece, Disposable, 1.01 OD, 2.625" L

    Sacroiliac (SI) Belt

    FDA UDI
    MEDICAL SPECIALTIES INCORPORATED·00802357633029·

    Sacroiliac Belt

    FDA UDI
    MEDICAL SPECIALTIES INCORPORATED·00802357000111·

    STEMPRO MSC SFM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SDIF DENTAL CHAIR WITH OPERATIVE UNIT AND ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Dental

    KYPHON XPEDE BONE CEMENT

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

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·March 17, 2020

    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

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 11, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 15, 2011

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 9, 2008

    KYPHON XPEDE BONE CEMENT

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

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·October 16, 2024

    1030489-2019-01511

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

    IKAZUCHI ZERO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·June 13, 2019

    1030489-2019-01423

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

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 19, 2019