BEUDAMED
    18 results · 36ms · 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.

    STS CORPORATION

    FDA registration
    STS CORPORATION·98 products·🇺🇸 United States

    8F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·December 15, 2017

    TERUMO ANGIO-SEAL 6 FRENCH STS PLUS

    FDA Adverse Event
    TERUMO MEDICAL CORP.·Product code MGB·December 22, 2022

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH BIOSCIENCE, INC.·Product code LCP·March 30, 2018

    RUNTHROUGH NS

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 27, 2018

    6F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code MGB·September 5, 2017

    8F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·May 25, 2017

    6F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code MGB·July 19, 2017

    6F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code MGB·July 14, 2017

    8F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·June 13, 2017

    6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE, US

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·June 12, 2017

    6F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL PRODUCTS·Product code MGB·May 2, 2017

    8FR ANGIO-SEAL STS PLUS OUS

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·June 15, 2017

    VOCSN

    FDA Adverse Event
    Injury ·VENTEC LIFE SYSTEMS, INC.·Product code CBK·February 13, 2025

    JaviTech e.K.

    Authorized representative
    🇩🇪 Germany·111 Manufacturers·1816 Devices

    Obelis s.a.

    Authorized representative
    🇧🇪 Belgium·546 Manufacturers·18515 Devices

    Wellkang Ltd

    Authorized representative
    259 Manufacturers·3500 Devices

    MedPath GmbH

    Authorized representative
    🇩🇪 Germany·537 Manufacturers·13464 Devices