Device Recall PKG, SCHERTEL FORCEPS, FENESTRATED,

  • Modelo / Serial
    42933 140481 143691 143692 244219 246731 246732 247405 640116 646137 646140 744912 744915 749912 840178 842220 842235 842238 842344 847887 847888 847889 847891 847892 847893 847894 847895 847899 848003 941360 941362 941363 941365 941366 941367 941368 941372 941373 941374 1044887 1046603 1046606 1047025 1047026 1047027 1140203 1142289 1142290 1143095 1143703 1144245 1144724 1144725 1144726 1144727 1144728 1145801 1146163 1146376 1146728 1146729 1146983 1147051 1240178 1240179 1240362 1240957 1242410 1244440 1245119 1245120 1245121 1245511 1340288 1340721 1340722 1341833 1342683 1343533 1343991 1343992 140404 162099
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA (nationwide) and Internationally to Algeria, Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, France, Germany, Greece, Guam, Guatemala, India, Italy, Japan, Jordan, Kuwait, Latin America, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Saudi Arabia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, and Venezuela.
  • Descripción del producto
    PKG, SCHERTEL FORCEPS, FENESTRATED, P/N 0250080312. || Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Stryker Endoscopy, 5900 Optical Ct, San Jose CA 95138-1400
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA