Establishment registration
JIANGYIN PUREMED
FDA establishment registration 3008352384 · Jiangyin Jiangsu, CN
Key facts
| Registration number | 3008352384 |
|---|---|
| Establishment name | JIANGYIN PUREMED |
| Owner/operator | Jiangyin PureMED Products CO., Ltd. |
| Owner/operator number | 10032092 |
| FEI number | 3008352384 |
| Address | 553-1 Huachang Road |
| City | Jiangyin Jiangsu |
| Country | CN |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | DWJ, FWZ, FYA, KKX, MDM, NOD, PUI |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- None 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