BEUDAMED
    22 results · 33ms · Sources: EU EUDAMED, US FDA

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    Polysmith Sleep System, Model NTI7593

    FDA 510(k)
    FDA Class 2 ·Neurology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517731746·CoRoent XL+, 16x18x50mm 15°

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1616500·16mm H x 16mm W x 50mm L x 0 degrees XLIF

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122261·Kwire .062x6" (1.6x150mm) Threaded

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122278·KWire .062x6" (1.6x150mm)

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L161650120·16mm H x 16mm W x 50mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X161650120·16mm H x 16mm W x 50mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X16165080·16mm H x 16mm W x 50mm L x 8 degrees XLIF

    IDS-ISYS CTX-1 (CROSSLAPS) CALIBRATION VERIFIERS, IDS-ISYS 25 HYDROXY VITAMIN D CALIBRATION VERIFIERS, AND IDS-ISYS...

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SELECT TENS, MODEL 4600S

    FDA 510(k)
    FDA Class 2 ·Neurology

    TROCHANTERIC NAIL KIT, TI GAMMA3 10X170MM X 125

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

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·May 20, 2014

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

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

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

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

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·June 11, 2013

    GREENSTONE

    FDA Adverse Event
    GREENSTONE LLC·Product code KZE·July 8, 2011

    PUMP MMT-715LNAB PRDGM INS V2.1 BL EN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·September 15, 2008

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 10, 2017

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022