Establishment registration
St. Jude Medical, Cardiology Division, Inc.
FDA establishment registration 3005334138 · Plymouth, US
Key facts
| Registration number | 3005334138 |
|---|---|
| Establishment name | St. Jude Medical, Cardiology Division, Inc. |
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| FEI number | 3005334138 |
| Address | 5050 Nathan Lane North |
| City | Plymouth |
| State | MN |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DQK, DQR, DQX, DQY, DRA, DRC, DRE, DRF, DRG, DRJ, DSK, DWZ, DXC, DXJ, DXO, DXY, DYB, GAX, GEI, GXD, GXI, IKD, ITX, IYN, IYO, JOQ, KGZ, KRG, LPB, LWP and 13 more |
| Device classes | 1, 2, 3 |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 10–99 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