BEUDAMED
    1,198 results · 23ms · Sources: EU EUDAMED, US FDA

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    TruPlan

    FDA 510(k)
    FDA Class 2 ·Radiology

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00195377046482·NTS Standard Tube, 22x120mm

    VITA TITANKERAMIK

    FDA UDI
    Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft·J017B2022120·VITA TITANKERAMIK COLOR OPAQUE, CO2, 12 g

    10PW - General Purpose

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588020129·10PW - General Purpose

    36M - Salt River Project-31 - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588022024·36M - Salt River Project-31 - Metal

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112816·BARRON VACUUM PUNCH 9.0MM

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS NORTH AMERICA LLC·Product code MHX·July 22, 2022

    MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PORTEX PERCUTANEOUS DILATATIONAL TRACHEOSTOMY KITS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·October 4, 2022

    MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 7, 2022

    MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 20, 2022

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·June 2, 2023

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·December 23, 2022

    DREAMSTATION AUTO BIPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS.INC·Product code BZD·May 19, 2022

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 27, 2014

    REPLY

    FDA Adverse Event
    Malfunction ·SORINGROUP ITALIA S.R.L.·Product code NVZ·June 28, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 5, 2011

    BD LUER-LOK SYRINGE 60 ML

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·October 7, 2019

    PLUM 360¿ INFUSER

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FRN·July 12, 2022