BEUDAMED
    13 results · 21ms · 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 ×

    Rebellion, Phantom Multi-Bite Kerrison Rongeur

    FDA 510(k)
    FDA Class 2 ·Neurology

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120694·Guidewire 2.5x230mm Partially Thrd

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120687·Guidewire 2.5x230mm Sgl Trocar

    devemed

    FDA UDI
    devemed GmbH·04061644030866·Dissecting tweezers, micro 1x2 / 0.6 mm, straig...

    MDK MULTI-APPLICATIONS PLATFORM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ISO-ELASTIC CERCLAGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 12, 2022

    ILET BIONIC PANCREAS

    FDA Adverse Event
    Malfunction ·BETA BIONICS, INC.·Product code QFG·April 28, 2026

    530G INSULIN PUMP MMT-751LNAS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 18, 2018

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORP·Product code LGW·November 13, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011

    ECHELON*FLEX45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 16, 2013

    XTEN

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·July 22, 2019