Gwowei Technology Co., Ltd.
Country not established
- Devices
- 2
What Gwowei Technology Co., Ltd. makes
Gwowei Technology Co., Ltd. manufactures the WELLGRAFT PE I and WELLGRAFT PE II, which are vascular grafts designed for peripheral arterial applications.
These devices are classified as Class II under US regulations and are listed in the FDA’s 510(k) registry. Gwowei Technology Co., Ltd. is based in the United States.
Catalogue
Wellgraft Pe I Ref K072444
Regimes: 510(k) Registry: 510(k)Wellgraft Pe Ii Ref K072170
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gwowei Technology Co., Ltd. have in the registry?
The registry currently lists 2 devices for Gwowei Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gwowei Technology Co., Ltd.'s devices?
Among its 2 most recently registered devices, Gwowei Technology Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gwowei Technology Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gwowei Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gwowei Technology Co., Ltd. in the registry?
The most recently registered devices listed for Gwowei Technology Co., Ltd. include WELLGRAFT PE I and WELLGRAFT PE II.