Establishment registration
SCIVITA MEDICAL TECHNOLOGY CO., LTD.
FDA establishment registration 3020746799 · suzhou Jiangsu, CN
Key facts
| Registration number | 3020746799 |
|---|---|
| Establishment name | SCIVITA MEDICAL TECHNOLOGY CO., LTD. |
| Owner/operator | SCIVITA MEDICAL TECHNOLOGY CO., LTD. |
| Owner/operator number | 10082577 |
| FEI number | 3020746799 |
| Address | No.2, Qingqiu Street, Suzhou Industrial Park, 215000 Suzhou, Jiangsu Prov., P.R.CHINA |
| City | suzhou Jiangsu |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | EOB, EOQ, FAJ, FCL, FET, FFL, FGB, FMH, GCJ, HET, HFB, HIF, HRX, IZI, LQR, NMH, NTN, NWB, OCY |
| 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