Skip to content

Results for “PRESSFT”

Registry
Country / market
More countries (1)
Risk class
More classes (11)
Verified

Category (EMDN)

Browse by category

38 devices foundsorted by relevance

Clear all

  • PressFT

    Conmed Corporation,United States
    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I

  • Genesys Pressft, Hi-Fi

    Conmed Corporation,United States
    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:III

  • PressFT

    Conmed Corporation,United States Group of variants
    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:IIa

  • Genesys Pressft NB261H

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:II

  • PressFT CNP211H

    Conmed Corporation,United States
    None Registry: GUDID Class:II

  • PressFT CNP261H

    Conmed Corporation,United States
    None Registry: GUDID Class:II

  • PressFT PGHS

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:I

  • Pressft NDB26H

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:I

  • Genesys Pressft NB211H

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:II

  • PressFT TD26H

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:I

  • PressFT CNB211H

    Conmed Corporation,United States
    None Registry: GUDID Class:II

  • PressFT TD21H

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:I

  • Pressft Ncoh

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:I

  • PressFT PGHC

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:I

  • PressFT PCOH

    Conmed Corporation,United States
    Withdrawn Registry: GUDID Class:I

  • PressFT CNB261H

    Conmed Corporation,United States
    Active Regimes: CE MDR CE MDD Registry: GUDID Class:II

  • Genesys Pressft Suture Anchor

    Linvatec Corporation d/b/a ConMed Linvatec,FDA registration: United States
    Active Regimes: CE MDR CE MDD 510(k) Registry: 510(k) Class:II

Showing 21-38 of 38