Establishment registration
SHENZHEN JIE BISHI TECHNOLOGY CO., LTD
FDA establishment registration 3034731361 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3034731361 |
|---|---|
| Establishment name | SHENZHEN JIE BISHI TECHNOLOGY CO., LTD |
| Owner/operator | Shenzhen Jie Bishi Technology Co., LTD |
| Owner/operator number | 10092220 |
| FEI number | 3034731361 |
| Address | Room 1208, Xinwei Building, No. 121 Jianhui Road, Yucui Community, Longhua Street, Longhua District |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | EAX, EFS, EJR, EMN, ERA, FLG, GBX, GDF, GFE, HOY, ISA, IWS, JEQ, JES, KAO, KMA, LJL, LWK, QJC |
| Device classes | 1 |
At a glance
- 10–99 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database