Device Recall PKG, 5MM INSERT, TENACULUM, 33CM,

  • Modèle / numéro de série
    44485 341728 541773 543282 742876 745131 845497 847458 940778 942549 942646 943423 943739 944093 944094 945232 946004 1040629 1040994 1041614 1042529 1043032 1044517 1046583 1140148 1141926 1142615 1144486 1145071 1145795 1146118 1147099 1240111 1240545 1241176 1242120 1242928 1244073 1244707 1246143 1340125 1343307 1343553 1345287 1345526 1345630 1346245 1346662 1440422 1440461 1441380 1442253
  • 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, 5MM INSERT, TENACULUM, 33CM, P/N 0250080698 || 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