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Results for “COLUMBUS”

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1,000+ devices foundsorted by relevance

  • 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    Withdrawn Registry: GUDID Class:II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    Withdrawn Registry: GUDID Class:II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 Ps NS114R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus NQ460

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® PS NN532

    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    Withdrawn Registry: GUDID Class:II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    Withdrawn Registry: GUDID Class:I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    Withdrawn Registry: GUDID Class:II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® PS NN515

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Ps NS119R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® CR DD NN255

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® CR/PS NN073K

    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    Withdrawn Registry: GUDID Class:II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    Withdrawn Registry: GUDID Class:I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 NE379R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® UC NN440

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR600M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® CR NN131

    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    Withdrawn Registry: GUDID Class:II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    Withdrawn Registry: GUDID Class:I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    Withdrawn Registry: GUDID Class:II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 NQ387R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR650M

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    Withdrawn Registry: GUDID Class:II