Devices

Device Recall PKG, 3MM PEEK MONOPOLAR HANDLE

Model / Serial
843744 847017 942768 943108 943436 943515 944197 944825 945711 1040927 1042098 1042468 1042513 1042514 1042957 1043819 1045057 1045626 1046584 1140930 1141656 1142239 1144237 1144342 1145343 1146674 1147037 1242641 1243948 1246163H 1340920H 1341894 1341894H 1344199 1344872 1344990 1345272 1345272H 1346215 1346215H 1346684 1440429 1441830
Device Class
2
Implanted device?
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.
Product Description
PKG, 3MM PEEK MONOPOLAR HANDLE, P/N 0250282045 || 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
Stryker Endoscopy
1 Event
- Recall of Device Recall PKG, 3MM PEEK MONOPOLAR HANDLE

Manufacturer

Stryker Endoscopy

Manufacturer Address
Stryker Endoscopy, 5900 Optical Ct, San Jose CA 95138-1400
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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