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Results for “COLUMBUS REVISION”

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747 devices foundsorted by relevance

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  • Columbus Revision NQ733R

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    Withdrawn Registry: GUDID Class:I

  • Columbus Revision F NP037R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR652M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR070K

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR103M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR613

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR615

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ753K

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR645M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR605

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR605M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR604M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ748R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR142M

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    Withdrawn Registry: GUDID Class:II

  • AS Columbus® REVISION F NR002Z

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NS142R

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    Withdrawn Registry: GUDID Class:I

  • Columbus Revision NQ755K

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    Withdrawn Registry: GUDID Class:I

  • Columbus Revision F NP062

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    Withdrawn Registry: GUDID Class:I

  • Columbus Revision NS116R

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

  • Columbus Revision NQ691R

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

Showing 681-700 of 747