BEUDAMED
    8 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.
    Filters Regulation: Us FDA ×

    SALMONELLA IFA*

    FDA 510(k)
    FDA Class 1 ·Hematology

    3M™ Forsus™

    FDA UDI
    3M UNITEK CORPORATION·00652221110473·3M™ Forsus™ Fatigue Resistant Device, 885-114, ...

    NUTRIENT BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    HOSKINS-BARKAN GONIOTOMY LENS 9MM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·June 19, 2014

    TRI-LOCK BPS SZ 2 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·October 22, 2010

    RADIUS VITALLIUM ROD 5.5 X 600 MM

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEAUX·Product code NKB·December 19, 2012

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020