INTERNAL JUGULAR PUNCTURE KIT

  • Modèle / numéro de série
    Lot Numbers: RF0018975, RF0022666, RF0063422, RF0087612, RF5107030, RF5119129, RF5129996, RF6012024, RF6034966, RF6046200, RF6068548, RF6079525, RF6081311, RF6103626, RF6127038, RF7019125, RF7032328, RF7065841, RF7090233, RF7102114, RF7124570, RF8020116, RF8020746, RF8033340, RF8057411, RF8072077, RF8084420, RF8108025, RF8122236, RF8123291, RF9014648, RF9039391, RF9042572, RF9070841, RF9097328 and RF9114810.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- United States - all 50 States, and the countries of Canada, South America, China, South Africa, Australia, Puerto Rico, Philippines, Singapore, South Korea, New Zealand, Mexico, Japan, India, Indonesia, Bahamas, Taiwan, Thailand, Finland, France, Cyprus, Czech Republic, Belgium, Germany, Ireland, Italy, Latvia, Netherlands, Poland, Slovakia, Spain, Bahamas, Costa Rico, Dominican Republic, Ecuador, Guatamala and the United Kingdom.
  • Description du dispositif
    INTERNAL JUGULAR PUNCTURE KIT with Blue FlexTip(R) Catheter/Product SKU (Code) AK-04050 || Internal jugular puncture kit
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Arrow International Inc, 2400 Bernville Road, Reading PA 19605
  • Société-mère du fabricant (2017)
  • Source
    USFDA

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