BEUDAMED
    8 results · 18ms · 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.

    NOVAMETRIX 350 RECORDER-PAPER CHART RECORDER

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    Hana/ProFx Traction Boot XLarge (pr)

    FDA UDI
    MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430106491·Left and Right boots

    QUANTIA LA(A)

    FDA 510(k)
    FDA Class 2 ·Immunology

    X-Suit NIR Biliary Metallic Stent

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

    X-SUIT NIR COVERED BILIARY METALLIC STENT

    FDA Adverse Event
    Malfunction ·MEDINOL LTD.·Product code FGE·December 27, 2017

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 5, 2014

    PROXIMATE*PPH PROCEDURE SET

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 1, 2010

    ENDOPATH** ETS45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 29, 2012