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Results for “COLUMBUS REVISION F”

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312 devices foundsorted by relevance

  • Columbus Revision F NP042

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR006K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR141

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR123

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision F NP041

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I
  • Columbus® REVISION F NR135M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR150

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR637

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR071K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR016K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR600

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR115M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR610

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR620

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR602M

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR135

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR623

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR120

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus® REVISION F NR646

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II
  • Columbus Revision F NS131R

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

Showing 221-240 of 312