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Results for “ARCADIUS XP C”

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149 devices foundsorted by relevance

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  • Arcadius Xp C ME514

    Aesculap Implant Systems, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:I

  • Arcadius Xp C ME520

    Aesculap Implant Systems, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C ME101T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO730P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO749P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C ME522

    Aesculap Implant Systems, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C ME099T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C ME100T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO769P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO793T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C ME121T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO772P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO707P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO729P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C ME122T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C US054R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C ME102T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C US068R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius Xp C US222R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C SO708P

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

Showing 121-140 of 149