BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    MAXI LD PTA BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CONNECTOR 22M - 22F + 6MM STEM

    FDA UDI
    Intersurgical Incorporated·05030267057375·CONNECTOR 22M - 22F + 6MM STEM

    TROCHANTERIC NAIL TRAY, LONG, Ø10mm x 130°

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665038996·

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190585·A/P Sizing and Distal Cutting Block Body Sub As...

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111123·FOX EYE SHIELD ALUMINUM

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108222·BARRAQUER NEEDLE HOLDER STRAIGHT W/ LOCK

    AMPLATZER TorqVue 45x45 Delivery Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ASTRA 2,3,4 AND 6: CHIP REVISION

    FDA 510(k)

    MAXPLUS EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·January 23, 2013

    KIMVENT

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK·Product code BSY·January 10, 2011

    ACCU-CHEK ® AVIVA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·July 29, 2014