BEUDAMED
    11 results · 23ms · 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 ×

    AMT Suture Delivery System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    VERTE-STACK® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074520841·SPACER 9193612 CRESCENT PEEK 36X12

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198383·AK3 PS Insert Trial Size 6, 12mm

    SYNGO.PLAZA

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIMENSION VISA ENZ 2 CAL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2014

    2.4MM CORTEX SCREW SELF-TAPPING 10MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·June 27, 2013

    IMPRESS ANGIOGRAPHIC CATHETERS

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·July 14, 2011

    LASSOSTARNAV,10P,15MM DIA LOOP

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DRF·February 22, 2023

    LASSOSTAR CATHETER

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER INC.·Product code DRF·December 30, 2020

    LASSOSTAR NAV CIRCULAR MAPPING CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·November 23, 2022