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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    SOMATOM X.cite, Scan&GO, SOMATOM go.Platform - go.Up, go.Now, go.Top, go.All, go. Sim, go. Open Pro, Scan&GO

    FDA 510(k)
    FDA Class 2 ·Radiology

    Trial Tibial Augment

    FDA UDI
    ADLER ORTHO SPA·08056269044172·TRIAL PANTHEON TIBIAL AUGMENT RM/LL SIZE 4 H5

    Pantheon System

    FDA UDI
    ADLER ORTHO SPA·08050880237791·Pantheon Salvage Cementless Stem L 115 Ø 24

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180102620·BIPOLAR RF-CABLE WITH WOLF INSTRUMENT CONNECTOR...

    BAILEY HEMOSTATIC FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896061019·BAILEY HEMOSTATIC FORCEPS ACUTE ANGLED EXTRA FI...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694006828·Plate to Bone Holding Forceps, Right

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776130251·BIPOLAR CABLE WITH WOLF CONNECTOR & DUAL BANANA...

    POLARIS ADJUSTABLE PRESSURE VALVE SHUNT

    FDA Adverse Event
    Other ·SOPHYSA·Product code JXG·December 13, 2005

    HARDYDISK, CEFOTAXIME 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PATIENTNET MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEEDLE 25GA 1IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·October 12, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 28, 2025

    SYNVISC

    FDA Adverse Event
    Injury ·GENZYME BIOSURGERY·Product code MOZ·March 15, 2005

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    UNICEL DXI WASH BUFFER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LDT·August 11, 2011

    TECNIS 1-PIECE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·July 1, 2013

    PORT-A-CATH PLASTIC HUB BENT NEEDLE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL, INC.·Product code LJT·September 21, 2015

    WALLSTENT ILIAC ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC IRELAND LTD.·Product code MAF·July 2, 2010

    PORT-A-CATH® PLASTIC HUB BENT NEEDLE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code LJT·September 21, 2015

    PORT-A-CATH® PLASTIC HUB BENT NEEDLE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code LJT·September 21, 2015