Shanghai Longmann Tech Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3018226067
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Shanghai Longmann Tech Co., Ltd. makes
Shanghai Longmann Tech Co., Ltd. manufactures the CuffTrek, a blood pressure monitoring device designed for clinical use.
The CuffTrek is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the US.
Catalogue
- Registry: GUDID
- Registry: GUDID
CuffTrek Ref K242642
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3018226067
- DUNS number
- 530703915
- Address
- Room 2106, No. 3, Lane 791, Lingling Road, Shanghai
Frequently asked questions
How many devices does Shanghai Longmann Tech Co., Ltd. have in the registry?
The registry currently lists 3 devices for Shanghai Longmann Tech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shanghai Longmann Tech Co., Ltd.'s devices?
Among its 3 most recently registered devices, Shanghai Longmann Tech Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Shanghai Longmann Tech Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Shanghai Longmann Tech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shanghai Longmann Tech Co., Ltd. in the registry?
The most recently registered devices listed for Shanghai Longmann Tech Co., Ltd. include CuffTrek LG-1 and CuffTrek.