Establishment registration
SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO. LTD.
FDA establishment registration 3003723176 · JINAN Shandong, CN
Key facts
| Registration number | 3003723176 |
|---|---|
| Establishment name | SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO. LTD. |
| Owner/operator | SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO. LTD. |
| Owner/operator number | 9050813 |
| FEI number | 3008801456 |
| Address | No.1 Shuangshan Sanjian Road, |
| City | JINAN Shandong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | FMK, KGX, KOX, NEC, QRK, QRL |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 100–999 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