BEUDAMED
    8 results · 22ms · 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 ×

    SEPTOJECT STERILE DISPOSABLE INJECTION NEEDLE

    FDA 510(k)
    FDA Class 1 ·Dental

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209104277·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111049378·LEFORT URETHRAL SOUND 24FR 11"

    LOCK-IT PLUS REGIONAL ANESTHESIA CATHETER SECUREMENT DEVICE, MODEL 100/399/216

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Dr. Yglo Skin Tag Remover

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SIGMA PS CEM FEM SZ2.5 R

    FDA Adverse Event
    Injury ·DEPUY IRELAND ¿ REG. # 9616671·Product code JWH·June 5, 2014

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·November 29, 2012

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - VASCULAR SOLUTIONS·Product code MGB·September 29, 2010