Establishment registration
DONNEVIE MEDICAL TECHNOLOGY (SHANGHAI) CO.LTD
FDA establishment registration 3015739059 · Shanghai, CN
Key facts
| Registration number | 3015739059 |
|---|---|
| Establishment name | DONNEVIE MEDICAL TECHNOLOGY (SHANGHAI) CO.LTD |
| Owner/operator | DonneVie Medical Technology (Shanghai) Co.Ltd |
| Owner/operator number | 10060970 |
| FEI number | 3015739059 |
| Address | Suite 101, 201 & 301,Bld 1, 138 Xinjun Ring, Minhang District |
| City | Shanghai |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | PUC |
| 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