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

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    Tamper Evident Cap

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAVIGATION MARKER, REFLECTIVE MARKER SPHERES

    FDA 510(k)
    FDA Class 2 ·Neurology

    FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

    EVIS EXERA III DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·February 18, 2022

    PS FEMORAL COMPONENT CLOSED BOX LGE RIGHT 74 MM CEMENTED

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code JWH·June 3, 2020

    PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

    KERRISON RONGEUR (40 DEG FWD), 4MM

    FDA Adverse Event
    Malfunction ·ABBOTT SPINE·Product code HTX·October 7, 2008

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 21, 2011

    HUT EXT DR FINAL ASSY-STANDARD

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code IXR·June 25, 2013

    MECTALIF POSTERIOR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

    PERF CON TIB BRG LRG 22X60

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    NON-POROUS PERF TIB TRAY-LGE

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    PERF ANAT TIBIAL STEM 120X14X5

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    MECTALIF OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X7 L0°

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·November 10, 2017

    MECTALIF (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI 11X22X7 L5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 29, 2020

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 23, 2019

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·May 25, 2023

    PEDICLE SCREW PEDICLE SCREW 6X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·September 21, 2018

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·October 17, 2018