BEUDAMED
    9 results · 21ms · 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 ×

    Flowtron ACS900

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LARGE BORE SPLITTABLE INTRODUCER KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACE DIRECT TOTALIRON-BINDING CAPACITY (TIBC) REAGENT, ACE SERUM IRON REAGENT, ACE LIPASE REAGENT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    VERSAFITCUP CC TRIO FLAT PE LINER 32 / E

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 14, 2021

    BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·October 6, 2014

    LEAD MODEL 304

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·June 3, 2013

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 29, 2011

    TECNIS

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·September 6, 2018

    TRANSMITTER MMT-7841ZW GST5G OUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code PQF·March 12, 2026