INTERNAL JUGULAR PUNCTURE KIT

  • Modelo / Serial
    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.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    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.
  • Descripción del producto
    INTERNAL JUGULAR PUNCTURE KIT with Blue FlexTip(R) Catheter/Product SKU (Code) AK-04050 || Internal jugular puncture kit
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Arrow International Inc, 2400 Bernville Road, Reading PA 19605
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA

Dispositivo con un nombre similar

Más información acerca de la data acá