Establishment registration
Shijiazhuang Aofeite Medical Device Co.,Ltd
FDA establishment registration 3009068676 · Shijiazhuang Hebei, CN
Key facts
| Registration number | 3009068676 |
|---|---|
| Establishment name | Shijiazhuang Aofeite Medical Device Co.,Ltd |
| Owner/operator | Shijiazhuang Aofeite Import and Export Co.,Ltd |
| Owner/operator number | 10034267 |
| FEI number | 3009068676 |
| Address | 2nd Floor, Building 3D, Liandong U-Valley Industrial Park, No.695 Tianshan South Street, High-tech Zone, |
| City | Shijiazhuang Hebei |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | FPF, HOY, HST, IKY, ILH, IME, ION, IOY, IPM, IPR, IQE, IQI, IQK, ISA, ISR, ITQ, ITW, KHA, KHY, KYR, KYS, LWF, LWG, LYG, MRI, MVV, NOC, OEA |
| Device classes | 1, U |
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