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Results for “PROSPACE”

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290 devices foundsorted by relevance

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  • Prospace® Xp SO110P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN054P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN186P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN147P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO148P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ233P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN007P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ258P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN039P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO137P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace FJ053R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I

  • Prospace® SN173P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN177P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO139P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace SJ210R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I

  • Prospace® SN172P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN107P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN160P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN008P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Prospace® SN011P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

Showing 101-120 of 290