Establishment registration
Isomedix Operations, Inc.
FDA establishment registration 2183744 · Minneapolis, US
Key facts
| Registration number | 2183744 |
|---|---|
| Establishment name | Isomedix Operations, Inc. |
| Owner/operator | STERIS Corporation |
| Owner/operator number | 1527821 |
| FEI number | 2183744 |
| Address | 380 90TH AVE NW |
| City | Minneapolis |
| State | MN |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | BSB, BSR, BTR, DPW, DQK, DQO, DQX, DQY, DRA, DRE, DRF, DSK, DSP, DSR, DTB, DTD, DTE, DWF, DWJ, DWP, DWS, DWZ, DXC, DXE, DXF, DXO, DYB, DYX, DZE, EMX and 245 more |
| Device classes | 1, 2, 3, f, N, U |
At a glance
- 100–999 Device listings
- None 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