Establishment registration
ANSELL HEALTHCARE PRODUCTS LLC
FDA establishment registration 3011209798 · Reno, US
Key facts
| Registration number | 3011209798 |
|---|---|
| Establishment name | ANSELL HEALTHCARE PRODUCTS LLC |
| Owner/operator | ANSELL HEALTHCARE PRODUCTS LLC |
| Owner/operator number | 8020065 |
| FEI number | 3011209798 |
| Address | 2301 Robb Drive |
| City | Reno |
| State | NV |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CCX, FZZ, GAX, IWP, KGO, KME, LYU, LYY, LYZ, LZA, LZC, MSH, NNW, OEA, OPJ, QDO |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 100–999 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