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

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    NEMUS 2 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    AGXO

    FDA UDI
    Oticon A/S·05707131261571·H110, BTE 13 WL 100 CBE AGXO

    Starbond CoS

    FDA UDI
    S & S Scheftner GmbH·04260207850501·Disc basic, 15 mm ø 98,3 mm / with edging

    Complete Cervical

    FDA UDI
    Seaspine Orthopedics Corporation·10889981040918·Screw - Self-Tapping - 3.5x17mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376694948·PROXIMITY FA SELF-TAP SCREW, 3.5 x 17mm

    Segmental Plating System

    FDA UDI
    ALPHATEC SPINE, INC.·00190376545813·SPS FA Self-Tap Screw, 3.5 x 17 mm

    SPINAL CONCEPTS INC. CADENCE AND TRAXIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRABECULAR METAL FEMORAL CONE AUGMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTWARE® VENTRICULAR ASSIST SYSTEM - CONTROLLER 1.0

    FDA Adverse Event
    Malfunction ·HEARTWARE·Product code DSQ·August 18, 2017

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172832·PS Tibia Insert Trial with Posterior Pin Relief...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144853·L UHMWPE PS Tibial Insert Sz C 17mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143818·L CIMA HXL PS Tibial Insert Sz C 17mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142958·L E-CIMA Vitamin E PS Tibial Insert Sz C 17mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147267·PS Tibia Insert Trial Size C, 17mm - Left

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 22, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015

    PENUMBRA SYSTEM JETD REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·May 8, 2019

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 30, 2015

    PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·June 14, 2015