Establishment registration
HANGZHOU KANGJI MEDICAL INSTRUMENT CO., LTD.
FDA establishment registration 3008843439 · HANGZHOU Zhejiang, CN
Key facts
| Registration number | 3008843439 |
|---|---|
| Establishment name | HANGZHOU KANGJI MEDICAL INSTRUMENT CO., LTD. |
| Owner/operator | Hangzhou Kangji Medical Instrument Co., Ltd. |
| Owner/operator number | 10033746 |
| FEI number | 3008843439 |
| Address | No. 1668 Chunjiang East Rd |
| City | HANGZHOU Zhejiang |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | EMF, FBM, FCL, FHO, FHQ, FMH, FSM, FZP, GAD, GCJ, GDI, GDM, GEA, GEI, HBQ, HBT, HCF, HFB, HGC, HIF, HTD, HTZ, KOH, LRC, LRW, MDM, NNQ |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1–9 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