BEUDAMED
    7 results · 18ms · 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.

    AUGUSTINE FIBEROPTIC LARYNGOSCOPE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    RUBBER LATEX SURGICAL GLOVES, STERILE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    INERPAN(TM) TEMPORARY WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    3002 MASTER BOMS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·December 7, 2012

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 6, 2010

    FLEXI-SEAL CONTROL FMS KIT US

    FDA Adverse Event
    Malfunction ·CONVATEC INC.·Product code KNT·May 15, 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