BEUDAMED
    28 results · 25ms · Sources: EU EUDAMED, US FDA

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    Resection Electrodes

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517244055·X-CORE 2 Ti Endcap, 16mm Rnd 0° Ø16

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702441536·Elvarex Forte 3/Thigh High/Slant, Closed Toe, E...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702616149·ELVAREX 2/KNEE HIGH/SLANT-OPEN TOE/SOFTFIT/CRAN...

    SureCore Semi-automatic Disposable Biopsy Needle

    FDA UDI
    Canyon Medical Inc.·06954414641202·Semi-automatic Disposable Biopsy Needle

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10885425499144·WEBSTER NEEDLE HOLDER

    Innomed, Inc.

    FDA UDI
    INNOMED, INC.·00840277130662·Olson Cannulated Swivel Tool Set

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)

    SureCore Semi-automatic Disposable Biopsy Needle

    FDA UDI
    Canyon Medical Inc.·06954414641240·Semi-automatic Disposable Biopsy Needle

    SureCore Semi-automatic Disposable Biopsy Needle

    FDA UDI
    Canyon Medical Inc.·06954414641356·Semi-automatic Disposable Biopsy Needle

    ARX SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216, INTELLIVUE PATIENT MONITORS MP5, MP2, X2 MODEL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    II Ring Retractor

    FDA UDI
    Automated Medical Products Corp.·00810118342394·Wylie Vein Retractor 1” x 8”

    II Ring Retractor

    FDA UDI
    Automated Medical Products Corp.·00810118342400·Wylie Vein Retractor 1” x 8” Aluminum/Radiolucent

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962162965·T-HANDLE, LARGE, WITH AO-QUICKCOUPLING LENGTH 1...

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    SENSIA SR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·October 10, 2014

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·June 11, 2013

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 14, 2011