BEUDAMED
    24 results · 22ms · Sources: EU EUDAMED, US FDA

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    INTERACTIVE MR LOCALIZER/ MAGNETOM OPEN AND OPEN VIVA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPSTONE® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994291035·SPACER 2990826 CAPSTONE PEEK 08X26

    COAGULATION ARP

    FDA 510(k)
    FDA Class 2 ·Hematology

    MONOBOND PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    CAPSTONE® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 16, 2013

    CAPSTONE® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code MAX·November 18, 2013

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·October 26, 2018

    CAPSTONE VERTEBRAL BODY SPACER

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MQP·October 1, 2009

    CAPSTONE VERTEBRAL BODY SPACER

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code MAX·June 18, 2009

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 31, 2017

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·March 5, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    CORNERSTONE-SR CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·March 21, 2025

    CORNERSTONE-SR CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·March 21, 2025

    CAPSTONE® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·November 19, 2025

    CAPSTONE® SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·July 21, 2023

    Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Sterile Co-Flex Med 4" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019