BEUDAMED
    8 results · 54ms · 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 FDA Adverse Event ×

    TRINITY STERILE INC

    FDA Adverse Event
    Malfunction ·TRINITY STERILE INC.·Product code KXF·March 8, 2007

    IV START KIT

    FDA Adverse Event
    Malfunction ·TRINITY STERILE, INC.·Product code LRS·January 8, 2009

    VAGINAL SPECULUM

    FDA Adverse Event
    Other ·TRINITY STERILE, INC.·Product code HDF·April 5, 2024

    VAGINAL SPECULUM

    FDA Adverse Event
    Other ·TRINITY STERILE, INC.·Product code HDF·April 5, 2024

    TRINITY IV START KIT WITH CHLORAPREP FREPP APPLICATOR

    FDA Adverse Event
    Injury ·TRINITY STERILE INC.·Product code FOZ·September 24, 2007

    KIT CAP CHANGE STERILE

    FDA Adverse Event
    Malfunction ·TRINITY STERILE, INC.·Product code OXQ·April 14, 2025

    DISPOSABLE VAGINAL SPECULUM

    FDA Adverse Event
    Malfunction ·TRINITY STERILE, INC.·Product code HIB·December 1, 2023

    CENTRAL LINE DRESSING KIT (SPECIFICALLY THE NON-ADHERENT PAD)

    FDA Adverse Event
    Injury ·TRINITY STERILE, INC.·Product code OXQ·July 7, 2022