BEUDAMED
    24 results · 37ms · 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 ×

    MICROSPEED EC MOTORSYSTEM GD650/GD653

    FDA 510(k)
    FDA Class 2 ·Neurology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776092733·Micro Clamp

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317361691·

    KALORE™

    FDA UDI
    Gc America Inc.·14548161291279·KALORE™ Unitips 10 Tips (0.16mL each) Shade CVT

    KALORE™

    FDA UDI
    Gc America Inc.·D0470036121·KALORE™ Unitips 10 Tips (0.16mL each) Shade CVT

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159008777·Micro Clamp

    QUASAR

    FDA UDI
    Modus Medical Devices Inc·G34350036120·MRI4D-10m cable

    OtoLase™ Straight HP

    FDA UDI
    LUMENIS LTD.·07290109142821·

    IABP (INTRA AORTIC BALLOON PUMP) UNKNOWN

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·August 29, 2025

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159029536·Micro Clamp

    PASCO MIC AND MIC/ID PANELS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ApeCord

    FDA UDI
    RIVERPOINT MEDICAL, LLC·00840277409768·Black UHMWPE Polyblend Non-Absorbable Suture

    ApeCord

    FDA UDI
    RIVERPOINT MEDICAL, LLC·00840277409775·White/Black UHMWPE Polyblend Non-Absorbable Suture

    ApeCord

    FDA UDI
    RIVERPOINT MEDICAL, LLC·00840277409744·Black UHMWPE Polyblend Non-Absorbable Suture

    ApeCord

    FDA UDI
    RIVERPOINT MEDICAL, LLC·00840277409751·White/Black UHMWPE Polyblend Non-Absorbable Suture

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 11, 2013

    ANEURXSTENT GRAFT (FLEXIBLE) WITH XPEDIENT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIO VASCULAR·Product code MIH·February 22, 2011

    CLEARSTAR PUMP

    FDA Adverse Event
    Malfunction ·ROSS PRODUCTS DIVISION·Product code LZH·February 20, 2008

    EQUINOXE REVERSE SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 22, 2024