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Results for “COLUMBUS”

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1,000+ devices foundsorted by relevance

  • AS Columbus® CR NN003Z

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR147

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® CR NN002K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® UC NN444

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR106

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • AS Columbus® CR NN012Z

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision NQ737R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® UC NN412

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® PS NN554

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • 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    Withdrawn Registry: GUDID Class:II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    Withdrawn Registry: GUDID Class:II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    Withdrawn Registry: GUDID Class:II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 NQ366R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus NQ880R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus NE242RM

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® PS NN168K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus NQ866R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR655M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus NQ870R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus Revision NQ735R

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    Withdrawn Registry: GUDID Class:I