Establishment registration
WENZHOU DONGFANG MEDICAL INSTRUMENTS CO., LTD
FDA establishment registration 3004784770 · WENZHOU Zhejiang, CN
Key facts
| Registration number | 3004784770 |
|---|---|
| Establishment name | WENZHOU DONGFANG MEDICAL INSTRUMENTS CO., LTD |
| Owner/operator | WENZHOU KINDCARE IMPORT & EXPORT CO.,LTD |
| Owner/operator number | 9066722 |
| FEI number | 3004784770 |
| Address | #143, Zhongxin Road, Wenzhou Industry Zone |
| City | WENZHOU Zhejiang |
| Country | CN |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | DXQ, ERA, FZY, GAX, HOY, LDE, LRW, LYU, MSH, OEA |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 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