BEUDAMED
    13 results · 35ms · 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.

    HOLDER FOR MODELS AF-10,1025,1040,5

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704539967·

    MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

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

    BellaTek Bars

    FDA 510(k)
    FDA Class 2 ·Dental

    TUMOR STENT DOUBLE LOOP URETERAL STENT KIT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·September 26, 2024

    HI-TORQUE WHISPER ES GUIDE WIRE

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·May 30, 2014

    ACCU-CHEK ® INFORM BASE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·November 20, 2012

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM DEXCOM SHARE SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 12, 2015

    BELLATEK HYBRID BAR 4 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·December 26, 2024

    BELLATEK HYBRID BAR 4 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·January 6, 2025

    BELLATEK¿ HYBRID BAR 5 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·February 18, 2025

    BELLATEK HYBRID BAR 5 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·March 18, 2025

    BELLATEK HYBRID BAR 4 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·January 6, 2025