Riverpoint Medical, LLC

3 dispositivos en la base de datos

  • Modelo / Serial
    Lot 120716-01
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    US Distribution in the states of: AZ, FL, and TX.
  • Descripción del producto
    Polyglycolic-Lactic Acid Absorbable Surgical Suture || Label reads in part "Coated VILET *** (Polyglacin 910) Suture UNDYED BRANDED V423 *** Riverpoint ***" || PGLA surgical suture is indicated for use in general soft tissue approximation and/or ligation, including use in opthalmic procedures, but not for use in cardiovascular and neurological tissues
  • Modelo / Serial
    Lot For Vet use: 160218-05V
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    US Nationwide distribution in the states of ID, MA, OR, NY and in the country of Australia.
  • Descripción del producto
    Polypropylene Surgical Sutures, brand Webglo, for vet use. Product is sterile. Part number: GP8665 || Product Usage: || For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.
  • Modelo / Serial
    Lot For human use:  160210-02.  Lots For Vet use:  160223-03V 160302-06V 160202-01V 160217-02V 160224-03V 160218-03V 160204-01
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    US Nationwide distribution in the states of ID, MA, OR, NY and in the country of Australia.
  • Descripción del producto
    Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: || 663BK || 663BL || 664BL || 928BK || Product Usage: || For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.

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Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ