BEUDAMED
    10 results · 22ms · 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 ×

    RAPIDEC CARBA NP

    FDA 510(k)
    FDA Class 2 ·Microbiology

    BI-METRIC HEAD/NECK HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304222809·

    BI-METRIC(R) HEAD/NECK PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304307728·

    NORFOLK MEDICAL NORPORT FAMILY OF PORTS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BLUE PTFE (FLUOROPLASTIC) VENTILATION TUBES

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    MPACT DOUBLE MOBILITY ACETABULAR SHELL Ø48

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·March 2, 2018

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 14, 2011

    ADVANTA 2 BED

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·May 30, 2013

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·September 9, 2008