BEUDAMED
    26 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 ×

    Nutricare Clear-ISOSAF Nasogastric Feeding Tube

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

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112922·CORNEAL TREPHINE BLADE7.75MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112502·BARRON VACUUM TREPHINE 7.75MM

    Blade Scalpel

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113462·SCLEROTOME BLADE #57 (BX/5)

    TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 46-815

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    100 S AND 100 LC AND 485 ANSER ULTRASOUND IMAGING SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 13, 2024

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·November 9, 2010

    BLOOD PUMP PU VALVES 25 ML, IN/OUT Ø9 MM

    FDA Adverse Event
    Injury ·BERLIN HEART GMBH·Product code DSQ·February 9, 2023

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    TSPACE PEEK IMPLANT 5 DEGREES 26X11.5X7MM

    FDA Adverse Event
    AESCULAP QG AND CO. KG·Product code MAX·June 21, 2013

    PURITAN BENNETT

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE PURITAN BENNETT·Product code CBK·October 10, 2008

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·August 4, 2011

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·July 14, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·July 14, 2025