BEUDAMED
    16 results · 35ms · Sources: EU EUDAMED, US FDA

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    Traxcess .007 Mini Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528104033·ExtremiFix Mid, 4.5 mm/5.5 mm Headed Screw Module

    NYOrtho Wheelchair Cushion Foam 16x18x3

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00811677019628·The NYOrtho Foam Wheelchair Cushions help preve...

    NYOrtho APEX CORE Coccyx Pommel Wheelchair Cushion Gel-Foam 16x18x3

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00810114601389·For patients requiring hip positioning and to e...

    NEWPORT E360 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STA - CONTROL LA 1+2

    FDA 510(k)
    FDA Class 2 ·Hematology

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026

    CLEARLINK CONTINU-FLO SOLUTION SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·December 6, 2021

    AXLE INTERSPINOUS FUSION SYSTEM TORQUE HANDLE

    FDA Adverse Event
    Injury ·X-SPINE SYSTEMS, INC.·Product code KWP·July 8, 2011

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 6, 2013

    ELEVESS

    FDA Adverse Event
    Other ·ANIKA THERAPEUTICS, INC.·Product code LMH·September 12, 2008

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 6, 2019

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·February 26, 2019

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·June 20, 2019

    SOEHENDRA STENT RETRIEVER

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code FGE·September 26, 2017