BEUDAMED
    99 results · 21ms · Sources: EU EUDAMED, US FDA

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    AltiVate Anatomic Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776116095·Pass Thru Bracket

    Avalign

    FDA UDI
    Avalign Technologies, Inc.·00190776119850·Pass Thru Bracket hole opening 6mm (.236"), sil...

    Avalign

    FDA UDI
    Avalign Technologies, Inc.·00190776020156·Pass Thru Bracket

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071150440·16F x 2.0cm MiniSPC Low Profile Suprapubic Cath...

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071147822·16F x 2.0cm MiniSPC Low Profile Suprapubic Cath...

    RPM RESPIRATORY GATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIMENSION VISTA DIGITOXIN, DIGOXIN, GENTAMICIN, N-ACETYLPROCAINAMIDE, PHENYTOIN, THEOPHYLLINE FLEX REAGENT CARTRIDGE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    NA

    FDA UDI
    Zimmer, Inc.·00889024084957·

    WEREWOLF RF 20000 CONTROLLER

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·June 29, 2020

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 11, 2013

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·July 12, 2011

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·July 8, 2008

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·December 6, 2018

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·December 6, 2018

    CONCERTO

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·December 2, 2024

    CONCERTO

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·December 2, 2024

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 11, 2020

    Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090

    FDA Recall
    Open, Classified ·Medtronic Inc.·Product code QAN·February 16, 2024

    TourniKwik Tourniquet Set (CFN 79012)

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code GDJ·May 16, 2024