SEERS.Co., Ltd
Country not established FDA FEI 3010222749
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3010222749
- DUNS number
- 557812763
- Address
- 291-13 Dongbudae-Ro, Pyeongtaek Gyeonggi
- Website
- seers.co.kr/lang_kr/
- facebook.com/mobicareseers
- [email protected]
- Phone
- +823180239821
Frequently asked questions
How many devices does SEERS.Co., Ltd have in the registry?
The registry currently lists 1 device for SEERS.Co., Ltd. Devices recorded under merged duplicate company entries are counted once.
Which registries list SEERS.Co., Ltd's devices?
Among its 1 most recently registered device, SEERS.Co., Ltd has devices listed in FDA GUDID (1 device).
What risk classes do SEERS.Co., Ltd's devices fall under?
Among its 1 most recently registered device, the classes recorded for SEERS.Co., Ltd's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SEERS.Co., Ltd in the registry?
The most recently registered devices listed for SEERS.Co., Ltd include Auto Blood Pressure Meter HX-461.