Research Endoscope Systems Intl.
Country not established
- Devices
- 1
What Research Endoscope Systems Intl. makes
Research Endoscope Systems Intl. manufactures suction-hemorrhoid ligators, devices used to treat hemorrhoids by applying ligatures to cut off blood flow.
The company’s portfolio is regulated under FDA Class II devices and is listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Suction-Hemorrhoid-Ligator Ref K832192
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Research Endoscope Systems Intl. have in the registry?
The registry currently lists 1 device for Research Endoscope Systems Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Research Endoscope Systems Intl.'s devices?
Among its 1 most recently registered device, Research Endoscope Systems Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Research Endoscope Systems Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Research Endoscope Systems Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Research Endoscope Systems Intl. in the registry?
The most recently registered devices listed for Research Endoscope Systems Intl. include SUCTION-HEMORRHOID-LIGATOR.