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

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    MOBILE MIM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517288714·CoRoent LC Ti, 12x9x30mm 8°

    DSPS® Cradle-S H MR

    FDA UDI
    MACROMEDICS B.V.·08719425700441·DSPS Cradle Type-S, High, MR safe

    N/A

    FDA UDI
    HANS RUDOLPH, INC.·00874750006953·8430A PNT/HTRSHELL/CONN ASSY

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776305123·Moynihan Towel Forceps. 2 x 2 prongs, 7.5" OL

    ACTIVE WASTE GAS SCAVENGER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROSTHESIS, ELBOW, HEMI-RADIAL, POLYMER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code KWI·January 25, 2017

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 14, 2013

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IKX·September 24, 2014

    BLADELESS VP 5MM SH W/FIXATION

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL·Product code GCJ·May 25, 2011

    RECONSTRUCTION NAIL R2.0, TI, LEFT T2 RECON Ø11X360 MM X 125°

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·July 23, 2018

    8MM TI STRAIGHT RADIAL STEM 28MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·January 24, 2017

    22MM COCR RADIAL HEAD STANDARD HEIGHT/12.5MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·January 24, 2017

    18MM COCR RADIAL HEAD STANDARD HEIGHT/11.5MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·September 7, 2017

    7MM TI STRAIGHT RADIAL STEM 26MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·September 7, 2017

    INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·July 21, 2021

    Model Number L231, PROPONENT DR EL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025