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Results for “COLUMBUS REVISION”

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  • Columbus® REVISION F NR136

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR158M

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    Withdrawn Registry: GUDID Class:II

  • AS Columbus® REVISION F NR012Z

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR655M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ735R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR156

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR632M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NS156R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR616

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ756K

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR600M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ680R

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    Withdrawn Registry: GUDID Class:I

  • Columbus® REVISION F NR144M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR650M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ745R

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    Withdrawn Registry: GUDID Class:I

  • Columbus Revision NQ739R

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    Withdrawn Registry: GUDID Class:I

  • AS Columbus® REVISION F NR074Z

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR648M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR622M

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    Withdrawn Registry: GUDID Class:II

  • Columbus Revision NQ689R

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

Showing 421-440 of 747