BEUDAMED
    8 results · 26ms · 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.

    6F ENVOY GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Adult Intraosseous Infusion Device

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·August 1, 2024

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NECLLCO·Product code CBK·February 25, 2013

    6 SHOOTER SAEED MULTI-BAND LIGATOR

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code MND·January 6, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OE MEDICAL SYSTEMS (SLC)·Product code JAA·July 24, 2014

    Z NAIL PF 14MM X 46CM UNIV Z NAIL GT 14MM X 46CM R Z NAIL GT 14MM X 46CM L Z NAIL TIBIA 14MM X 38CM UNIV Z NAIL TIBIA 14MM X 40CM UNIV Z NAIL TIBIA 14MM X 42CM UNIV Z NAIL TIBIA 14MM X 44CM UNIV

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·June 21, 2017