BEUDAMED
    9 results · 23ms · 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.

    COMPLEMENT C4 FOR THE TECHNICON DPA-1(TM) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65888826211·ANGIO PACK

    STRADIS HEALTHCARE

    FDA UDI
    STRADIS MEDICAL, LLC·M75288826210·

    CrossFT Knotless Deep Thread Suture Anchor with Disposable Driver

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EMIT-STM ETHYL ALCOHOL ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 19, 2014

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 26, 2010

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·Product code NIQ·December 20, 2012

    HUMAPEN SAVVIO 3ML (PINK)

    FDA Adverse Event
    Injury ·ELI LILLY AND COMPANY·Product code FMF·October 3, 2019