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Results for “PROSPACE”

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290 devices foundsorted by relevance

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  • Prospace® SN153P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN084P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN017P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN028P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN072P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN032P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN038P

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    Withdrawn Registry: GUDID Class:II

  • Prospace SJ876R

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    Withdrawn Registry: GUDID Class:I

  • Prospace® SN187P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN190P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN145P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO109P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN060P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ285P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN087P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ234P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO130P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN128P

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    Withdrawn Registry: GUDID Class:II

  • ProSpace™ DBM Moldable Putty (Jar) ME915

    Xtant Medical Holdings, Inc.,FDA registration: United States
    None Registry: GUDID Class:II

  • Prospace® Xp SO129P

    Aesculap, Inc.,FDA registration: United States
    Active Regimes: CE MDR Registry: GUDID Class:II

Showing 201-220 of 290