Establishment registration
ZHEJIANG ORIENT GENE BIOTECH
FDA establishment registration 3008517993 · Huzhou Zhejiang, CN
Key facts
| Registration number | 3008517993 |
|---|---|
| Establishment name | ZHEJIANG ORIENT GENE BIOTECH |
| Owner/operator | Zhejiang Orient Gene Biotech Co., Ltd |
| Owner/operator number | 10033347 |
| FEI number | 3008517993 |
| Address | 3787 East Yangguang Avenue |
| City | Huzhou Zhejiang |
| Country | CN |
| Establishment types | Repackager/relabeler, Complaint file establishment |
| Registration valid through | 2026 |
| Product codes listed | CDM, CEK, CEN, CET, CHH, CKA, DIC, DIO, DIS, DJC, DJG, DJR, DKZ, FMH, GQG, GTY, JGY, JHN, JIL, JIN, JIO, JIR, JJB, JJE, JJH, JJI, JJQ, JLO, JMA, JMT and 57 more |
| Device classes | 1, 2, N, U |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 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