BEUDAMED
    44 results · 22ms · 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 ×

    pjur WOMAN Nude pjur med SENSITIVE glide

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Waterlase Laser Tips

    FDA UDI
    Biolase, Inc.·00647529000809·A tip kit containing 30 single-use MZ Zip tips ...

    MAYO SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055568·MAYO SCISSORS CURVED BEVELED BLADES POWER CUT B...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034678·2.0/2.4 Screwdriver Shaft, Long, Manual

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471159101·Niti Thermal Tri-Force Nat Dimp 020X020 Lo

    RONGEUR NASAL SEPTUM

    FDA UDI
    W.H. Holden, Inc.·D9282007300·

    IMPOAID

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

    ORION NASAL CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD CONVENTIONAL NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FMI·September 29, 2023

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·July 20, 2019

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·July 20, 2019

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·July 20, 2019

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·July 20, 2019

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·July 20, 2019

    WALLFLEX ENTERAL DUODENAL STENT

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code MUM·February 26, 2009

    ASKU

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·November 15, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·November 15, 2011

    ANGIO-SEAL STS PLUS DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·November 20, 2008

    LTV

    FDA Adverse Event
    Malfunction ·CAREFUSION 203, INC·Product code CBK·October 24, 2014

    1.85MM TI MATRIX SCREW SELF-DRILLING

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code JEY·April 14, 2011