BEUDAMED
    10 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.

    HESSBURG GLIDE UNTRAOCULAR LENS GUIDES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209114290·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111207549·GUYON SOUND W/O THREAD 29FR

    NaturaLase CO2 Laser System

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

    E-2320 PA S

    FDA 510(k)
    FDA Class 2 ·Radiology

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 16, 2019

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2014

    ULTRACISION** HARMONIC SCALPEL** CURVED SHEARS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·October 4, 2010

    QWIX FIXATION SCREW 4.3 DIAMETER X 40MM LENGTH

    FDA Adverse Event
    Malfunction ·NEWDEAL SAS·Product code HWC·November 15, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 14, 2019