BEUDAMED
    13 results · 24ms · 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 ×

    Merit ONE Snare System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Reveal

    FDA UDI
    Oticon A/S·05707131343833·G10, MINIRITE 312 2.4G C090 REVEAL

    URI-CATH

    FDA UDI
    UTAH MEDICAL PRODUCTS, INC.·H67141935070·Urinary Drainage and Collection Set with a Sili...

    MEDICAL VISORS MV100

    FDA 510(k)
    FDA Class 2 ·Radiology

    OLYMPUS CHF TYPE Y0003

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

    CONTOUR PLUS ELITE

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·August 22, 2024

    BD Microtainer SST- Amber Part/Catalog Number: 365978

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Company·October 16, 2019

    CONTOUR PLUS ELITE

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·July 1, 2023

    TRIDENT 10 X3 INSERT 32MM ID

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·October 8, 2008

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 27, 2013

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·July 13, 2011

    CONTOUR® NEXT

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·November 10, 2023

    CONTOUR® NEXT

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·October 23, 2023