Suzhou CellPro Biotechnology Co., Ltd.
Country not established FDA FEI 3017178434
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
- Authorised rep.
- Lotus NL B.V.NL
- Authorised rep.
- SUNGO Europe B.V.NL
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3017178434
- DUNS number
- 554551042
- Address
- Building 1, CECEP (Suzhou) , Environmental Technology Industrial Park, Suzhou Jiangsu
Frequently asked questions
How many devices does Suzhou CellPro Biotechnology Co., Ltd. have in the registry?
The registry currently lists 1 device for Suzhou CellPro Biotechnology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Suzhou CellPro Biotechnology Co., Ltd.'s devices?
Among its 1 most recently registered device, Suzhou CellPro Biotechnology Co., Ltd. has devices listed in FDA GUDID (1 device).
What risk classes do Suzhou CellPro Biotechnology Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Suzhou CellPro Biotechnology Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Suzhou CellPro Biotechnology Co., Ltd. in the registry?
The most recently registered devices listed for Suzhou CellPro Biotechnology Co., Ltd. include Cellpro 802021E01-233.