Establishment registration
PT. Nipro Indonesia Jaya
FDA establishment registration 3010377171 · Karawang Jawa Barat, ID
Key facts
| Registration number | 3010377171 |
|---|---|
| Establishment name | PT. Nipro Indonesia Jaya |
| Owner/operator | NIPRO CORPORATION |
| Owner/operator number | 8030375 |
| FEI number | 3010377171 |
| Address | Kawasan Industri Suryacipta, Jl. Surya Utama Kav. I 22B, 23 & 24 |
| City | Karawang Jawa Barat |
| Country | ID |
| Registration valid through | 2026 |
| Product codes listed | FJK, FMF, FMI, KDI |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 100–999 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