BEUDAMED
    7 results · 25ms · 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.

    THE LEWIS TUBE HOLDER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR

    FDA 510(k)
    FDA Class 2 ·Microbiology

    BRAIN PORT

    FDA 510(k)
    FDA Class 2 ·Neurology

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 17, 2013

    ENTRUST AT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·December 13, 2010

    VERITY ADX SR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014

    Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015