Establishment registration
TIDI PRODUCTS, LLC
FDA establishment registration 2182318 · NEENAH, US
Key facts
| Registration number | 2182318 |
|---|---|
| Establishment name | TIDI PRODUCTS, LLC |
| Owner/operator | TIDI PRODUCTS, LLC |
| Owner/operator number | 9921057 |
| FEI number | 2182318 |
| Address | 570 Enterprise Dr |
| City | NEENAH |
| State | WI |
| Country | US |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | BSK, BWN, CAT, CBH, CCW, EAJ, ECB, EFN, EGZ, EIA, EYJ, EYQ, FLL, FME, FMP, FMQ, FNL, FOK, FRG, FRL, GDX, GEI, IKX, IQI, IYO, JEQ, KGX, KHR, KIA, KME and 16 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 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