Establishment registration
CITOTEST Labware Manufacturing CO., LTD.
FDA establishment registration 3010420046 · Haimen Jiangsu, CN
Key facts
| Registration number | 3010420046 |
|---|---|
| Establishment name | CITOTEST Labware Manufacturing CO., LTD. |
| Owner/operator | CITOTEST LABWARE MANUFACTURING CO., LTD. |
| Owner/operator number | 9077486 |
| FEI number | 3010420046 |
| Address | No.339 Beihai West Road |
| City | Haimen Jiangsu |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | FMA, FMH, FNY, GHC, GHK, GJW, HYB, HYK, HYL, IBJ, IBK, IBL, IDR, IDS, IDW, IDZ, JQC, JRB, JRC, JRL, JRO, JRQ, JSG, JSM, KDT, KEO, KER, KES, KET, KEW and 16 more |
| Device classes | 1 |
At a glance
- 10–99 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