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Results for “COLUMBUS”

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  • Columbus Sling E-clip Soft

    Human Care HC AB,Sweden Group of variants
    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Columbus Revision

    Aesculap AG,Germany
    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Columbus Revision F

    Aesculap AG,Germany Group of variants
    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Columbus NQ472R

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    Withdrawn Registry: GUDID Class:I

  • AS Columbus® PS NN163Z

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR017K

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    Withdrawn Registry: GUDID Class:II

  • Columbus® CR NN930K

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    Withdrawn Registry: GUDID Class:II

  • Columbus® CR DD NN1221

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    Withdrawn Registry: GUDID Class:II

  • Columbus® CR NN830K

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR127M

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    Withdrawn Registry: GUDID Class:II

  • Columbus NQ887R

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    Withdrawn Registry: GUDID Class:I

  • AS Columbus® REVISION F NR013Z

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR111M

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR074K

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    Withdrawn Registry: GUDID Class:II

  • Columbus® REVISION F NR155M

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    Withdrawn Registry: GUDID Class:II

  • Columbus NQ398

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    Withdrawn Registry: GUDID Class:I

  • Columbus NQ370R

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    Withdrawn Registry: GUDID Class:I