BEUDAMED
    9 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.

    DENTURE CLEANSING TABLET

    FDA 510(k)
    FDA Class 1 ·Dental

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704294194·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771050268·Steinmann Pins, Single trocar threaded, 5/32-in...

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771015765·Steinmann Pins, Single trocar threaded, 5/32-in...

    WowGoHealth Blood Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE, HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE WITH SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 13, 2014

    LAG/COMP SCREW

    FDA Adverse Event
    Injury ·SMITH-NEPHEW INC.·Product code JDS·October 15, 2010

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·December 13, 2012