BEUDAMED
    9 results · 28ms · 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.

    BEAR NICU-1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Stainless Steel Wire

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746047251·WIRE SS LOWER 016 FORM II 50/PK

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209125265·

    syngo Application Software VD11

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO: DP-9900 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, MODEL DP-9900

    FDA 510(k)
    FDA Class 2 ·Radiology

    PICCOLO XPRESS CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·ABAXIS·Product code JJG·August 23, 2024

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·May 27, 2014

    SYNCHRON LX® I 725 CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·October 5, 2010

    10MM TI LATERAL ENTRY FEMORAL RECON NAIL-EX/440MM/LT-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HWC·November 30, 2012