BEUDAMED
    8 results · 18ms · 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 ×

    COMFIT STERILE LATEX EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690129936·PS-C Insert, Size 5 x 13mm

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

    MEDCOMP VASCU-SHEATH INTRODUCER SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLEARED UNDER GRAFTON II EDBM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·November 16, 2010

    EEA 28MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC·Product code GAG·January 14, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 5, 2014