BEUDAMED
    81 results · 28ms · Sources: EU EUDAMED, US FDA

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    DURETTE IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    EXCITE DSC

    FDA 510(k)
    FDA Class 2 ·Dental

    NIPRO HYPODERMIC NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RENAL UROLOGY STENT K072293

    FDA Adverse Event
    Other ·FOSSA MEDICAL INC·Product code FAD·April 10, 2014

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·November 29, 2019

    CAPSTONE VERTEBRAL BODY SPACER

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 3, 2017

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code KWP·November 14, 2018

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·January 22, 2020

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 22, 2021

    PS FEMORAL COMPONENT CLOSED BOX LGE RIGHT 74 MM CEMENTED

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

    CAPSTONE CAGE

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code MAX·November 19, 2015

    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 MAX·July 2, 2009

    CAPSTONE SYSTEM

    FDA Adverse Event
    Malfunction ·SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·September 3, 2010

    CAPSTONE® SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·April 17, 2014

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·October 18, 2017

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MAX·December 21, 2009

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X45 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·April 23, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·July 11, 2008

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·May 1, 2011