BEUDAMED
    356 results · 19ms · 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 ×

    CONSENSUS ACETABLAR SHELL, TI COATED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717101519·Burs FG 8, Pkg/10

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036019389·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450311431·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450239568·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450156063·

    ULTRASONIC NEBULIZER, MODEL NE-520

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARTHRO-SURGIMAT-A103

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISION XTRA / OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·May 25, 2007

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 25, 2013

    5.0MM TI LOCKING HEAD SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KTT·March 7, 2011

    BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).

    FDA Enforcement
    Class II ·Ongoing·Becton Dickinson & Co.·July 2, 2025

    ACCU-CHEK GUIDE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code NBW·March 9, 2020

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026