Youcare Technology Co., Ltd. (Wuhan)
ChinaFDA applicant, unverified
- Devices
- 2
What Youcare Technology Co., Ltd. (Wuhan) makes
Youcare Technology Co., Ltd. manufactures single-use ureteral access sheaths and introducer needles, designed for urological procedures. These devices facilitate catheter insertion and drainage in clinical settings.
The company’s products are classified as Class II and Unclassified (U) devices under FDA regulations, with records submitted via the 510(k) pathway. The manufacturer is based in Wuhan, China, with devices listed in the US regulatory system.
Catalogue
Disposable Ureteral Access Sheath Ref K230748
Regimes: 510(k) Registry: 510(k)Introducer Needle Ref K222705
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Youcare Technology Co., Ltd. (Wuhan) have in the registry?
The registry currently lists 2 devices for Youcare Technology Co., Ltd. (Wuhan). Devices recorded under merged duplicate company entries are counted once.
Which registries list Youcare Technology Co., Ltd. (Wuhan)'s devices?
Among its 2 most recently registered devices, Youcare Technology Co., Ltd. (Wuhan) has devices listed in FDA 510(k) (2 devices).
What risk classes do Youcare Technology Co., Ltd. (Wuhan)'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Youcare Technology Co., Ltd. (Wuhan)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Youcare Technology Co., Ltd. (Wuhan) in the registry?
The most recently registered devices listed for Youcare Technology Co., Ltd. (Wuhan) include Disposable Ureteral Access Sheath and Introducer Needle.