Shenzhen Deliduo Medical Technology Co., Ltd
ChinaFDA applicant, unverified FDA FEI 3019865183
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Shenzhen Deliduo Medical Technology Co., Ltd makes
Shenzhen Deliduo Medical Technology Co., Ltd manufactures electrode pads, which are reusable medical devices used for electrotherapy applications such as transcutaneous electrical nerve stimulation (TENS) or muscle stimulation therapies.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Electrode Pad Ref K241512
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3019865183
- Address
- Room B1406, Block B, Phase 3, Hongji Garden, Center City Area 4, Jixiang Community, Shenzhen City Guangdong
Frequently asked questions
How many devices does Shenzhen Deliduo Medical Technology Co., Ltd have in the registry?
The registry currently lists 1 device for Shenzhen Deliduo Medical Technology Co., Ltd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shenzhen Deliduo Medical Technology Co., Ltd's devices?
Among its 1 most recently registered device, Shenzhen Deliduo Medical Technology Co., Ltd has devices listed in FDA 510(k) (1 device).
What risk classes do Shenzhen Deliduo Medical Technology Co., Ltd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Shenzhen Deliduo Medical Technology Co., Ltd's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shenzhen Deliduo Medical Technology Co., Ltd in the registry?
The most recently registered devices listed for Shenzhen Deliduo Medical Technology Co., Ltd include Electrode Pad.