BEUDAMED
    10 results · 27ms · 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.

    HYPER PULSE INTERMITTENT TOPICAL OXYGEN CHAMBER C-100, CB-100

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

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000337315·CANNULA 963-777 3.2 MM DIAMETER

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00673978963365·INST 963-777 CANNULA, 3.2 MM DIAMETER

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000055448·CANNULA 963-777, 3.2 MM DIAMETER

    ABLE GLOVE NITRILE BLUE POWDER FREE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    B-WRAP

    FDA 510(k)

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·February 15, 2013

    11.0 CM LONG ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·July 29, 2014

    ETHICON ENDO LINER CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 12, 2011

    Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene Liner Component (Product Line: 350-21-XX, 350-22-XX); b. Vantage Mobile-Bearing Polyethylene Liner Component (Product Line: 350-41-XX, 350-42-XX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021