Establishment registration
MEDTRONIC VASCULAR
FDA establishment registration 1220452 · DANVERS, US
Key facts
| Registration number | 1220452 |
|---|---|
| Establishment name | MEDTRONIC VASCULAR |
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| FEI number | 1220452 |
| Address | 37A Cherry Hill Dr |
| City | DANVERS |
| State | MA |
| Country | US |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | DQO, DQX, DQY, DTL, DXE, KRA, LIT, LWP, MAV, NKE, NVZ, OJX, QEZ |
| Device classes | 2, 3 |
At a glance
- 10–99 Device listings
- 1,000+ 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