Establishment registration
MEDTRONIC PERFUSION SYSTEMS
FDA establishment registration 2184009 · Minneapolis, US
Key facts
| Registration number | 2184009 |
|---|---|
| Establishment name | MEDTRONIC PERFUSION SYSTEMS |
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| FEI number | 1000116158 |
| Address | 7611 Northland Dr |
| City | Minneapolis |
| State | MN |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CAC, DPT, DQY, DRA, DRF, DRY, DTL, DTM, DTN, DTP, DTQ, DTR, DTS, DTW, DTY, DTZ, DWA, DWE, DWF, DWS, DXS, FLL, FMH, FQH, FZX, GAD, GCY, GDJ, GEI, GFT and 16 more |
| Device classes | 1, 2 |
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