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Results for “COLUMBUS REVISION”

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  • AS Columbus® REVISION F NR001Z

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR610M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR126

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision F NS127R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR631

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR079K

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR622

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NS141R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR101M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR151M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ766K

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    Withdrawn Registry: GUDID Class:I

  • Columbus Revision NQ742R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR113

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ749R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR611

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR127

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR633

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ763K

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR621M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ730R

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

Showing 581-600 of 747