BEUDAMED
    10 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.

    TENS-O-MATIC

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950031191·ADAPTER 1/4" FEMALE NDT/EMPEAS

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334012403·VanBuren Sound, curved, 1-3/4" nominal bend hei...

    10PC - UP - 380-54620 - Locamotive

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588110127·10PC - UP - 380-54620 - Locamotive

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0110120·Sounder, Ball Tip, Straight, Soft

    POWDER FREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SYNTHETIC VINYL EXAMINATION GLOVES, POWDER FREE (BLUE/GREEN) (AND MULTIPLE LABELS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    U BY KOTEX CLICK SUPER AND REGULAR TAMPONS

    FDA Adverse Event
    Malfunction ·AVENT S. DE R.L. DE C.V.·Product code HEB·August 10, 2010