BEUDAMED
    57 results · 23ms · Sources: EU EUDAMED, US FDA

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    DIGITAL THERMOMTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950024193·PROBE LACRIMAL BOWMAN STERLING SIZE 00-0 5" 13C...

    SCOTT'S SELECT K-FILES 6/pk 25mm # 20

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77811225201·ENDODONTIC K-FILES (6/pack) Length: 25mm, Size:...

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113768·PS-C Insert, Size 5 x 20mm

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450191439·

    U2 ACETABULAR CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD NEXIVA CLOSED IV CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NOVASURE IMPEDANCE CONTROLLED EA SYSTEM

    FDA Adverse Event
    Injury ·HOLOGIC·Product code MNB·May 16, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 26, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 13, 2011

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 1, 2020

    GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 9, 2025

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 23, 2022

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·Product code FOZ·June 25, 2021

    BD VACUTAINER® LH PST¿ II PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 5, 2023

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 28, 2019

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 3, 2025

    RADIFOCUS GUIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 12, 2024

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·August 30, 2023

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·August 7, 2020