Manufacturers

Disetronic Medical Systems, Inc.

32 dispositifs dans la base de données

Device Recall Dtron
  • Modèle / numéro de série
    Lots 06010107, 06030242, 06040085, 06050110 and 06060126.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide and Canada.
  • Description du dispositif
    Disetronic D-TRONplus Insulin Pump Battery Pack; Ref/Catalog no. 04697014001.
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).
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).
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).
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).
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Disetronic Medical Systems, Inc.
  • Adresse du fabricant
    Disetronic Medical Systems, Inc., 11800 Exit 5 Pkwy Ste 120, Fishers IN 46037-7989
  • Source
    USFDA