BEUDAMED
    17 results · 22ms · Sources: EU EUDAMED, US FDA

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    BRIDALVEIL Occipital Cervical Thoracic System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169595958·TRIAL 2171250 O25 IB 20MM 6 DEG 10X50

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517292797·CoRoent® XLFW, 12x22x50mm Lordotic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293173·

    LuxaPrint Ortho Flex 385

    FDA UDI
    DMG Digital Enterprises SE·D9821712500·(Meth) acrylate-based light-curing resin for th...

    AOS HUMERAL NAIL 7.0mm x 25cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016857·

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100769·FLIERINGA FIXATION RING 15MM

    CA, MODEL: CAM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GIVEN PILLCAM PLATFORM WITH PILLCAM SB CAPSULES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TROCHANTERIC NAIL KIT, TI GAMMA3 10X170MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 14, 2012

    GMK EFFICIENCY TRIAL KEEL S5-6

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·April 20, 2018

    HERMETIC LUMBAR CATHETER, CLOSED TIP

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·September 27, 2018

    HT COMMAND

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·June 14, 2013

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 1, 2011

    FREESTYLE FREEDOM

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 19, 2008

    OSS CEMENTED IM STEM 13X150

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 9, 2020

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018