BEUDAMED
    97 results · 38ms · Sources: EU EUDAMED, US FDA

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    NEEDLE, AIR ASPIRATOR 16 GA MODIFIED W/GREEN CAP

    FDA UDI
    NOVOSCI CORP.·B0662010100000·A sterile, sharp bevel-edged, hollow tubular me...

    NEEDLE, AIR ASPIRATOR 16 GA MODIFIED W/GREEN CAP

    FDA UDI
    NOVOSCI CORP.·B066201010NS1·A sharp bevel-edged, hollow tubular metal instr...

    CT9000 ADV DOMESTIC BASIC SYS

    FDA Adverse Event
    Injury ·LIEBEL-FLARSHEIM CO.·Product code DXT·February 2, 2006

    FARADRIVE STEERABLE SHEATH CLEAR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRA·June 27, 2025

    BARD® POLYURETHANE URETERAL CATHETERS, OPEN TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EYB·May 3, 2019

    BARD® POLYURETHANE URETERAL CATHETERS, OPEN TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EYB·December 21, 2023

    ANGIOMAT ILLUMENA

    FDA Adverse Event
    Injury ·LIEBEL-FLARSHEIM CO.·Product code DXT·March 13, 2008

    WATCHMAN FXD CURVE? ACCESS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·January 14, 2026

    ACIST

    FDA Adverse Event
    Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·August 13, 2019

    ACIST

    FDA Adverse Event
    Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·November 9, 2012

    2 UNIT RED CELL SET W/RC2H FIL

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORPORATION·Product code GKT·October 28, 2021

    FG GATEWAY OTW OUS 2.00MM X 9MM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MINN·Product code GBA·November 14, 2014

    WATCHMAN TRUSTEER? ACCESS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·December 26, 2025

    WATCHMAN FXD CURVE? ACCESS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·June 25, 2025

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM ¿ SINGLE PORT 20 GA 1.25 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 22, 2022

    FOGARTY ARTERIAL EMBOLECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES PR·Product code DXE·May 4, 2016

    PALL POSIDYNE NEO FILTER

    FDA Adverse Event
    Malfunction ·PALL LIFE SCIENCES PUERTO RICO, LLC·Product code FPB·April 13, 2009

    12F MODIFIED Tesio CATHETER SET, REF MCTC1235SM, UDI 884908027259 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Enforcement
    Class II ·Terminated·Medical Components, Inc dba MedComp·March 28, 2018

    BD INSYTE¿ AUTOGUARD¿ BC PRO SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 18, 2022

    Pediatric Air Aspirator Needle manufactured by Novosci Corp., The Woodlands, TX

    FDA Recall
    Terminated ·Novosci Corp·Product code GAA·November 24, 2003