Sgmp Co., Ltd.
Country not established FDA establishment FEI 3003069816
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Sgmp Co., Ltd. makes
SGMP CO., LTD. manufactures a non‑sterile, powder‑free medical device.
The device is classified as Class I and is listed in the FDA 510(k) registry. The company is based in Thailand.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Non-Sterile Powder-Free Ref K000868
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003069816
- Address
- 181 MOO 6, TAMBOL KAMPAENGPHET, Hatyai Songkhla
Frequently asked questions
How many devices does SGMP CO., LTD. have in the registry?
The registry currently lists 1 device for SGMP CO., LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SGMP CO., LTD.'s devices?
Among its 1 most recently registered device, SGMP CO., LTD. has devices listed in FDA 510(k) (1 device).
What risk classes do SGMP CO., LTD.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for SGMP CO., LTD.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SGMP CO., LTD. in the registry?
The most recently registered devices listed for SGMP CO., LTD. include NON-STERILE POWDER-FREE.