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

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    syngo.CT Cardiac Planning

    FDA 510(k)
    FDA Class 2 ·Radiology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047540·RELINE-O Trial,11mm H Offset Right L-pop

    Pantheon System

    FDA UDI
    ADLER ORTHO SPA·08050880237722·Pantheon Salvage Cementless Stem L 115 Ø 15

    Positioner / Compressor

    FDA UDI
    Treace Medical Concepts, Inc.·00810111226691·LIGHTNING BLOCK - PROXIMAL LEFT

    METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055223·METZENBAUM SCISSORS STRAIGHT TUNGSTEN CARBIDE P...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153160236·SCREWDRIVER BLADE

    PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150,

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THERASPHERE

    FDA Adverse Event
    Injury ·MDS NORDION·Product code KXK·July 15, 2005

    TUNA THERAPY (PROSTIVA)

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code GEI·May 1, 2008

    TUNA THERAPY (PROSTIVA)

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code GEI·May 1, 2008

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·March 7, 2006

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·June 4, 2019

    DRILL ATTACHM 45° CANN W/JACOBS CHUCK F/

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·October 24, 2014

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·July 1, 2013

    S-ROM*SLEEVE PRX ZTT, 18F-XXL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·February 20, 2013

    SYRINGE 0.3ML 8MM 90 BX 450 MO

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·August 17, 2020

    PEDICLE SCREW MUST COMBINED SETSCREW H4-T27 - (4X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·September 26, 2024

    MECTALIF TRANSFORAMINAL CAGES TIPEEK

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·April 25, 2025