Establishment registration
HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD
FDA establishment registration 9616872 · QIANJIANG, HUBEI, CN
Key facts
| Registration number | 9616872 |
|---|---|
| Establishment name | HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD |
| Owner/operator | HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD |
| Owner/operator number | 9041777 |
| FEI number | 3002897187 |
| Address | YUANGUANG ROAD. |
| City | QIANJIANG, HUBEI |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DWL, DYN, ECB, EFN, EHZ, EIC, EYJ, EYQ, FMA, FME, FMW, FQM, FRG, FRK, FRL, FSM, FXP, FXX, FYF, GDY, HMP, ILG, ILI, IPM, ITG, IWO, JOJ, KDD, KGX, KHA and 22 more |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 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