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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 US055R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius Xp C ME402R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius Xp C US058R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius Xp C ME524

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C ME111T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C US093R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C SO768P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C ME115T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C US057R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius Xp C US214R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C SO706P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO727P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius® Xp C SO710P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C US059R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius Xp C US198R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C ME105T

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C US213R

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C SO752P

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    Withdrawn Registry: GUDID Class:II

  • Arcadius Xp C ME516

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    Withdrawn Registry: GUDID Class:I

  • Arcadius® Xp C SO746P

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    Withdrawn Registry: GUDID Class:II

Showing 61-80 of 149