BEUDAMED
    8 results · 17ms · 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.

    ENDOLAP INSUFFLATOR TUBING SET

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Sierra

    FDA UDI
    Seaspine Orthopedics Corporation·10889981095239·Occipital Tap, 10mm

    Equashield Closed System drug Transfer Device (CSTD)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Dorado™ PTA Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL- NEUROMODULATION·Product code LGW·February 6, 2013

    LC PCA III INFUSER

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code MEA·December 9, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 22, 2014

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026