Establishment registration
Midwest Medical Mfg
FDA establishment registration 3007589160 · Oakland, US
Key facts
| Registration number | 3007589160 |
|---|---|
| Establishment name | Midwest Medical Mfg |
| Owner/operator | MIDWEST MEDICAL MFG |
| Owner/operator number | 10029313 |
| FEI number | 3007589160 |
| Address | 9614 Oakland Rd |
| City | Oakland |
| State | AR |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | HMR, HNF, HNQ, HNR |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None 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