Establishment registration
Zhejiang Mateside Medical Devices Technology Co., Ltd
FDA establishment registration 3016678950 · Ningbo Zhejiang, CN
Key facts
| Registration number | 3016678950 |
|---|---|
| Establishment name | Zhejiang Mateside Medical Devices Technology Co., Ltd |
| Owner/operator | Zhejiang Mateside Medical Devices Technology Co., Ltd |
| Owner/operator number | 10062787 |
| FEI number | 3016678950 |
| Address | Room 10-1, 10-2, 10-3, 10-4, Building 30, No. 300 Desheng Road, Zhanqi Town, Yinzhou District |
| City | Ningbo Zhejiang |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | BXB, EYQ, FMR, FNG, FNJ, FNL, FNM, FRZ, FSA, IKK, ILS, IMR, INM, INN, INO, IOR, IQK, ISA, ITJ, KMN, LLI |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1–9 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