Establishment registration
Merrimack Manufacturing
FDA establishment registration 3044561902 · Manchester, US
Key facts
| Registration number | 3044561902 |
|---|---|
| Establishment name | Merrimack Manufacturing |
| Owner/operator | Merrimack Manufacturing |
| Owner/operator number | 10062587 |
| FEI number | 3044561902 |
| Address | 350 Gay St |
| City | Manchester |
| State | NH |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | NDC, QFG |
| Device classes | 2 |
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