BEUDAMED
    307 results · 52ms · Sources: EU EUDAMED, US FDA

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    SKIN STAPLER 35W

    FDA Adverse Event
    Injury ·TELEFLEX LLC·Product code QQS·December 23, 2025

    MICRO PUNCTURE KIT

    FDA Adverse Event
    Injury ·TELEFLEX LLC·Product code DYB·August 1, 2024

    SKIN STAPLER 35W

    FDA Adverse Event
    Injury ·TELEFLEX LLC·Product code QQS·August 9, 2024

    SKIN STAPLER 35W

    FDA Adverse Event
    Injury ·TELEFLEX LLC·Product code QQS·August 9, 2024

    SKIN STAPLER 35W

    FDA Adverse Event
    Injury ·TELEFLEX LLC·Product code QQS·August 9, 2024

    SKIN STAPLER 35W

    FDA Adverse Event
    Injury ·TELEFLEX LLC·Product code QQS·August 9, 2024

    HUDSON RCI

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC·Product code BTR·July 3, 2023

    VASCBAND

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC.·Product code DXC·November 4, 2024

    WECK

    FDA Adverse Event
    Malfunction ·TELEFLEX, LLC·Product code HAO·January 29, 2026

    BITEGARD BITE BLOCK

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC·Product code BRW·March 25, 2025

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·May 17, 2024

    ARROW PRESSURE INJECTABLE ARROWG+ARD BLUE PLUS THREE-LUMEN CVC

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC (NADC)·Product code FOZ·August 1, 2024

    AC3 OPTIMUS IABP CONSOLE

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC (NADC)·Product code DSP·May 7, 2026

    TELEFLEX NITINOL GUIDEWIRE

    FDA Adverse Event
    Injury ·TELEFLEX LLC (NADC)·Product code DQX·August 28, 2023

    CHEST TUBE SYSTEM

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC (NADC)·Product code KDQ·August 28, 2025

    TITANIUM LIGATION CLIP MEDIUM BLUE

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC (NADC)·Product code FZP·February 9, 2023

    O'REILLY ESOPHAGEAL RETRACTOR

    FDA Adverse Event
    Injury ·TELEFLEX LLC (NADC)·Product code KAL·December 5, 2022

    MICRO PUNCTURE SET

    FDA Adverse Event
    Malfunction ·TELEFLEX / TELEFLEX LLC·Product code DYB·January 29, 2026

    ARTERIAL CATHETERIZATION KIT

    FDA Adverse Event
    Malfunction ·TELEFLEX LLC (NADC)·Product code DQX·March 26, 2026

    CATHETER, INTRAVASCULAR, THERAPEUTIC, LONG-TERM GREATER THAN 30 DAYS

    FDA Adverse Event
    Other ·TELEFLEX LLC (NADC)·Product code LJS·March 30, 2026