BEUDAMED
    8 results · 19ms · 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.

    LIFE-AIR 1000 PATIENT WARMING COVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ventura NanoMetalene System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981152178·Ventura NM Trial, 11mm x 28mm x 14mm, Lordotic

    SP NEWTRON MODULE

    FDA 510(k)
    FDA Class 2 ·Dental

    CHLORASHIELD IV DRESSING WITH CHG ANTIMICROBIAL

    FDA 510(k)
    FDA Unclassified ·Unknown

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    EBCIOR BREAST BIOPSY PROBE

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 3, 2014

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEURMODULATION·Product code LGW·December 16, 2010

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 29, 2013