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Results for “COLUMBUS REVISION”

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747 devices foundsorted by relevance

  • Columbus Revision F NQ631R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR123M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR630M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR116

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR156M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NS157R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus Revision NQ752K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR148

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NQ704R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR104

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR112

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR635M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR632

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR154M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR637M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR141M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • AS Columbus® REVISION F NR072Z

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR621

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NQ764K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR146

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

Showing 501-520 of 747