Devices

Device Recall Disetronic

  • Modèle / numéro de série
    Lot 3J012UF.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
  • Description du dispositif
    Disetronic Ultraflex 8/110 infusion set; (Distributed outside of the US only).
  • Manufacturer
    Disetronic Medical Systems, Inc.
  • 1 Event

Fabricant

Disetronic Medical Systems, Inc.
  • Adresse du fabricant
    Disetronic Medical Systems, Inc., 11800 Exit 5 Parkway, Suite 120, Fishers IN 46038
  • Source
    USFDA

4 dispositifs médicaux avec un nom similaire

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Device Recall Disetronic DTron
  • Modèle / numéro de série
    All units with the following lot numbers being used by patients 13 years of age or younger: lots 4013674 through 4022628. The last affected lot expires in April 2007.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide.
  • Description du dispositif
    Disetronic D-Tronplus Insulin Pump adapters; Ref 3000803; catalog reference number 0457243001 sold in packages of ten adapters.
  • Manufacturer
    Roche Diagnostics Corp.
Device Recall Disetronic
  • Modèle / numéro de série
    Lot 3H003UF.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
  • Description du dispositif
    Disetronic Ultraflex 8/60 infusion set; (Distributed outside of the US only).
  • Manufacturer
    Disetronic Medical Systems, Inc.
Device Recall Disetronic
  • Modèle / numéro de série
    Lot 3G039UF.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
  • Description du dispositif
    Disetronic Ultraflex 8/80 infusion set; Catalog number 4489039001. (Distributed outside of the US only).
  • Manufacturer
    Disetronic Medical Systems, Inc.
Device Recall Disetronic
  • Modèle / numéro de série
    Lot 3H067UF.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
  • Description du dispositif
    Disetronic Ultraflex 10/110 infusion set; (Distributed outside of the US only).
  • Manufacturer
    Disetronic Medical Systems, Inc.