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Results for “COLUMBUS REVISION”

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747 devices foundsorted by relevance

  • AS Columbus® REVISION F NR005Z

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR004K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR100M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR100

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR603

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NS148R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • AS Columbus® REVISION F NR017Z

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR143

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR077K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR635

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NQ640R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR130M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NQ685R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR143M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR644

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR152M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR654

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NS128R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR104M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR653

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

Showing 561-580 of 747