Establishment registration
HEMAGEN DIAGNOSTICS, INC.
FDA establishment registration 1181055 · Baltimore, US
Key facts
| Registration number | 1181055 |
|---|---|
| Establishment name | HEMAGEN DIAGNOSTICS, INC. |
| Owner/operator | HEMAGEN DIAGNOSTICS, INC. |
| Owner/operator number | 1221107 |
| FEI number | 1181055 |
| Address | 2900 LOCH RAVEN RD |
| City | Baltimore |
| State | MD |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CEL, CEO, CIC, CIG, CIX, DBM, DCK, DHN, DHR, DLJ, GGW, GLZ, GMS, GNP, GOK, GPW, GQH, GQO, GRA, GRE, JFJ, JHM, JIS, JIT, JJG, JJQ, JJY, KHS, KLI, KLS and 13 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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