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

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    Connector System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RENU REPROCESSED NELLCOR OXIMETRY SENSOR, MODEL D-25, N-25

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SOLCART B

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

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·October 18, 2017

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·February 13, 2020

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·April 11, 2022

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 18, 2024

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT,

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·November 16, 2018

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·November 13, 2018

    CAPSTONE PTC SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 8, 2020

    GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 3 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 29, 2019

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·December 7, 2017

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·April 1, 2020

    CRESCENT SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·October 11, 2021

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·March 22, 2019

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·January 7, 2019

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·June 15, 2011

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 18, 2008

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·July 10, 2020