Establishment registration
NIPRO VASCULAR CORPORATION Aichi Facility
FDA establishment registration 3030042169 · Seto Aichi, JP
Key facts
| Registration number | 3030042169 |
|---|---|
| Establishment name | NIPRO VASCULAR CORPORATION Aichi Facility |
| Owner/operator | NIPRO VASCULAR CORPORATION |
| Owner/operator number | 10061300 |
| FEI number | 3030042169 |
| Address | 1-176 Shiokusagaoka |
| City | Seto Aichi |
| Country | JP |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | PNO |
| Device classes | 2 |
At a glance
- 1–9 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