Establishment registration
Ortho Clinical Diagnostics, K.K.
FDA establishment registration 3012963943 · Harumi, Chuo-ku Tokyo, JP
Key facts
| Registration number | 3012963943 |
|---|---|
| Establishment name | Ortho Clinical Diagnostics, K.K. |
| Owner/operator | QuidelOrtho Corporation |
| Owner/operator number | 2024674 |
| FEI number | 3012963943 |
| Address | Harumi Prime Square 15F, 2-1-40 |
| City | Harumi, Chuo-ku Tokyo |
| Country | JP |
| Registration valid through | 2026 |
| Product codes listed | CDN, CDP, CDT, CDZ, CEC, CEM, CEW, CFJ, CFN, CFT, CGA, CGJ, CGN, CGR, CHH, CIG, CIT, CIW, CIX, CJE, CJY, CZW, DAD, DBI, DCF, DCK, DDG, DDR, DEM, DGR and 83 more |
| Device classes | 1, 2, N, U |
At a glance
- 100–999 Device listings
- 1,000+ 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