BEUDAMED
    3,416 results · 34ms · 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 ×

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902113068·Pressure Injectable ARROWg+ard Blue PLUS(R) Mul...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902113051·Pressure Injectable ARROWg+ard Blue PLUS(R) Mul...

    THERMOCOOL® SMARTTOUCH® SF BI-DIRECTIONAL NAV CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·August 4, 2015

    COLS

    FDA Adverse Event
    Malfunction ·FH INDUSTRIE·Product code MBI·October 31, 2017

    INJECTOR LUER LOCK N35

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code ONB·September 10, 2024

    CA500, EPIX UNIVERSAL CLIP APPLIER 3/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code FZP·March 8, 2022

    GC80

    FDA Adverse Event
    Injury ·SAMSUNG ELECTRONICS CO., LTD.·Product code KPR·June 22, 2017

    SYRINGE 10ML SALINE XS

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code FMF·September 27, 2021

    OPTIFLUX 180NR DIALYZER FINISHED ASSMBLY

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·October 24, 2023

    THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·January 13, 2015

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE SPECIALIZED ORTHOPEDICS·Product code PGN·April 14, 2022

    SOUNDSTAR

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code OBJ·April 3, 2025

    ENSITE VELOCITY¿ SYSTEM AMPLIFIER

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code DQK·February 22, 2023

    C-ARMOR DRAPE

    FDA Adverse Event
    Malfunction ·TIDI PRODUCTS LLC·Product code KKX·July 15, 2022

    PLMA DVC V11.51 1 N

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·October 31, 2014

    SPINNING SPIROS® CLOSED MALE LUER, PURPLE CAP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code ONB·August 3, 2023

    CADD MEDICATION CASSETTE RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code FPA·July 16, 2025

    BD SYRINGE 3ML LL EURO 200 S/C

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 20, 2026

    BD SYRINGE 5ML LL EURO 125 S/C

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 20, 2026

    VERSACARE FRAME

    FDA Adverse Event
    Injury ·HILL-ROM BATESVILLE·Product code FNL·June 1, 2018