BEUDAMED
    1,216 results · 31ms · 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 ×

    MULTILINE; DLY-1

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MULTILINE; DLY-1

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Bio Compression Systems Multi-Flo DVT Model IC-1545-DLI

    FDA UDI
    Bio Compression Systems, Inc·00812311022042·

    Amico Diagnostic Station

    FDA UDI
    Amico Diagnostic Incorporated·00697077002268·Diag. Station -Oph & Oto LED, Disp, L-Brkt Anro...

    Amico Diagnostic Station

    FDA UDI
    Amico Diagnostic Incorporated·00697077001094·Diag. Station -Oph & Oto, Disp.,L-Brkt Aneroid ...

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·May 5, 2026

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·February 21, 2025

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 21, 2025

    FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SENSOR

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC·Product code MDS·June 16, 2020

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·November 12, 2021

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·May 27, 2026

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 29, 2020

    I-STAT EG7+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·October 6, 2020

    DEXCOM G7

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 26, 2026

    FREESTYLE LIBRE 3 PLUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code QBJ·August 14, 2025

    FREESTYLE LIBRE 3 PLUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code QBJ·August 14, 2025

    FREESTYLE LIBRE 3 PLUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code QBJ·August 14, 2025

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·December 31, 2020

    Puritan Bennett KnightStar 330 Bi-Level Ventilator, Catalogue Numbers: Y-KS330-NA, Y-KS330-SD, DSY-KS330-NA, DSY-K5330-SD, DLY-KS330-NA & DLY-KS330-SD

    FDA Recall
    Terminated ·Puritan Bennett Corporation·Product code MNT·August 31, 2006

    ONE TOUCH ULTRA MINI METER

    FDA Adverse Event
    Injury ·LIFE SCAN·Product code NBW·October 4, 2017