BEUDAMED
    13 results · 39ms · 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 ×

    HMS PURPLE AND BLACK HEPARIN CARTRIDGES & CONTROL

    FDA 510(k)
    FDA Class 2 ·Hematology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707059905·DB BRACKET 31 EXTREMO NO-Ni 22

    Pinnacle

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730010933·Pinnacle 022 Roth U/L 5x5 Hks 345, OS Pad U/L 4...

    Pinnacle®

    FDA UDI
    Ortho Organizers, Inc.·00190707112875·Pinnacle .022 Roth U/L 5x5 Hks 345, OS Pad U/L ...

    Votion®

    FDA UDI
    Ortho Organizers, Inc.·00190707114800·Votion .022 Roth U/L 5x5 Hks 345, OS Pad U/L 4/...

    Votion

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730009104·Votion 022 Roth U/L 5x5 Hks 345, OS Pad U/L 4/5...

    NARKOMED MRI-2 ANESTHESIA SYSTEM, MODEL NM-MRI-2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NEXTRA TI HAMMERTOE CORRECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918173061·Gown_Set-In sleeve_Standard_X-Large_Extra long_...

    BARDIA FOLEY CATHETER SILICONE COATED K922431

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·November 1, 2021

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·January 4, 2013

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code DTB·July 9, 2014