Establishment registration
BEIJING HONGDEE CORPORATION
FDA establishment registration 3011898560 · Beijing, CN
Key facts
| Registration number | 3011898560 |
|---|---|
| Establishment name | BEIJING HONGDEE CORPORATION |
| Owner/operator | BEIJING HONGDEE CORPORATION |
| Owner/operator number | 10050774 |
| FEI number | 3011898560 |
| Address | Suite 402, Bldg No 7 |
| City | Beijing |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DQA, FLL, FZM, HJB, HJF, HJG, HJI, HJL, HJO, HKL, HKM, HKN, HKO, HKQ, HKW, HKY, HKZ, HLF, HLH, HLI, HLJ, HLM, HLS, HMD, HMF, HMH, HOS, HOX, HPA, HPC and 13 more |
| Device classes | 1, 2 |
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