Device Recall PKG, SPRING HANDLE

  • Modèle / numéro de série
    413144 414465 614433 716055 717057 717566 913220 913565 913566 913625 913763 914558 914559 914560 914654 914655 915026 915062 915269 915270 915430 915791 915895 1013200 1013201 1013277 1013393 1014635 1015163 1015164 1015774 1015863 1016125 1016405 1016407 1016555 1016556 1113333 1113334 1113335 1113340 1114205 1114544 1114545 1114546 1115529 1115530 1115650 1115652 1115653 1116111 1116113 1116460 1116461 1117176 1117177 1213128 1213258 1213259 1213973 1213975 1214001 1214735 1214736 1215298 1215299 1216023 1216024 1216228 1216229 1216288 1216721 1216722 1313330 1313331 1313332 1313805 1313806 1313947 1313948 1313972 1314203 1314204 1314472 1315785 1315786 1315787 1410413
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    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.
  • Description du dispositif
    PKG, SPRING HANDLE, P/N 0250080237. || 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

Fabricant

  • Adresse du fabricant
    Stryker Endoscopy, 5900 Optical Ct, San Jose CA 95138-1400
  • Société-mère du fabricant (2017)
  • Source
    USFDA