BEUDAMED
    8 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.

    NEWPORT VENTILATOR MODEL E100

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DISPOSABLE POWDER FREE VINYL EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BIRD TBIRD VELA VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BIVONA CUSTOM FLEXTEND TTS TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INC.·Product code JOH·May 1, 2014

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 6, 2012

    ECHELON 60 ENDOPATH STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·September 20, 2007

    Philips Azurion system; Software Version Number: R3.1;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·January 28, 2026

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015