Establishment registration
SHENZHEN MEI ZHI GUANG DIAN LIMITED
FDA establishment registration 3019778249 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3019778249 |
|---|---|
| Establishment name | SHENZHEN MEI ZHI GUANG DIAN LIMITED |
| Owner/operator | SHENZHEN MEI ZHI GUANG DIAN LIMITED |
| Owner/operator number | 10094450 |
| FEI number | 3019778249 |
| Address | 301 and 101, Building D, Jingtie Industrial Park, No. 49, Changjiang Pu Road, Heao Community, Yuanshan Street, |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | ILY |
| Device classes | 2 |
At a glance
- 1–9 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