BEUDAMED
    7 results · 25ms · 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.

    MICRO-AIRE DISPOSABLE MINI & MAXI LAVAG

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNITY IS PATIENT VIEWER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·July 1, 2019

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 6, 2012

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LIGATING CL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code FZP·September 13, 2007

    AVANCE

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA·Product code BSZ·April 10, 2014