Wuhan W.E.O Science & Technology Development Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Wuhan W.E.O Science & Technology Development Co., Ltd. makes
The company manufactures single-use infusion sets, including standard and extended-length versions, as well as precision infusion filters designed for controlled fluid delivery in medical applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: CE MDR 510(k) Registry: EUDAMED510(k)
Frequently asked questions
How many devices does Wuhan W.E.O Science & Technology Development Co., Ltd. have in the registry?
The registry currently lists 1 device for Wuhan W.E.O Science & Technology Development Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wuhan W.E.O Science & Technology Development Co., Ltd.'s devices?
Among its 1 most recently registered device, Wuhan W.E.O Science & Technology Development Co., Ltd. has devices listed in EUDAMED (1 device) and FDA 510(k) (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Wuhan W.E.O Science & Technology Development Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wuhan W.E.O Science & Technology Development Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wuhan W.E.O Science & Technology Development Co., Ltd. in the registry?
The most recently registered devices listed for Wuhan W.E.O Science & Technology Development Co., Ltd. include Infusion Sets with Precision Filter for Single Use, Precision Infusion Filter for Single Use, Extended Infusion Sets for Single Use.