Establishment registration
DOUBLE WHITE MEDICAL TECHNOLOGY DEVELOPMENT(GUANGZHOU) CO. LTD.
FDA establishment registration 3037591931 · GUANGZHOU Guangdong, CN
Key facts
| Registration number | 3037591931 |
|---|---|
| Establishment name | DOUBLE WHITE MEDICAL TECHNOLOGY DEVELOPMENT(GUANGZHOU) CO. LTD. |
| Owner/operator | Double White Medical Technology Development(Guangzhou) Co. L |
| Owner/operator number | 10093182 |
| FEI number | 3037591931 |
| Address | Room 505, No. 222(Self-edited: 616)Jianshe North Road, Xinhua Street, Huadu District |
| City | GUANGZHOU Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | EHM, MAU |
| Device classes | 1 |
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