BEUDAMED
    22 results · 33ms · Sources: EU EUDAMED, US FDA

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    PIVO 20G

    FDA UDI
    VELANO VASCULAR, INC.·00850984007003·PIVO 20G compatible device. Formerly TIVA.

    PIVO 20G

    FDA UDI
    VELANO VASCULAR, INC.·00850984007027·PIVO (2.0) 20G compatible device.

    PIVO 22G

    FDA UDI
    VELANO VASCULAR, INC.·00850984007010·PIVO 22G Compatible device

    PIVO 22G

    FDA UDI
    VELANO VASCULAR, INC.·00850984007034·PIVO (2.0) 22G Compatible device

    PIVO 24G

    FDA UDI
    VELANO VASCULAR, INC.·00850984007089·24G Compatible PIVO Blood draw device

    Velano Vascular Q2 Extension Set

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Velano Vascular Blood Collection Adapter

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EXT¿ STABILIZED EXTENSION SET WITH NEARPORT¿ IV ACCESS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·June 12, 2023

    VELANO VASCULAR Q2 EXTENSION SET

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code FPA·November 12, 2019

    STABILIZED 201-0006 EXT EXTENSION SET

    FDA Adverse Event
    Malfunction ·VELANO VASCULAR·Product code FPA·June 15, 2023

    TUBES, VIALS, SYSTEMS, SERUM SEPARATORS, BLOOD COLLECTION

    FDA Adverse Event
    Malfunction ·VELANO VASCULAR·Product code JKA·October 13, 2022

    PIVO

    FDA Adverse Event
    Malfunction ·VELANO VASCULAR·Product code JKA·November 19, 2019

    VELANO VASCULAR Q2 EXTENSION SET

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC·Product code FPA·October 22, 2019

    VELANO VASCULAR Q2 EXTENSION SET

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code FPA·October 18, 2019

    PIVO 20G

    FDA Adverse Event
    Malfunction ·VELANO VASCULAR, INC.·Product code JKA·June 21, 2023

    PIVO 22G

    FDA Adverse Event
    Malfunction ·VELANO VASCULAR, INC.·Product code JKA·September 23, 2022

    BD MICROCLAVE® STABILIZED EXTENSION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·June 30, 2023

    PIVO Blood Collection Device 20G, REF: 202-0005

    FDA Recall
    Terminated ·Velano Vascular·Product code JKA·November 10, 2021

    PIVO Blood Collection Device 20G, REF: 202-0005

    FDA Enforcement
    Class II ·Terminated·Velano Vascular·February 2, 2022

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·September 13, 2024