Establishment registration
GUANGZHOU HEHONG BIOTECH CO., LTD.
FDA establishment registration 3043639843 · Guangzhou Guangdong, CN
Key facts
| Registration number | 3043639843 |
|---|---|
| Establishment name | GUANGZHOU HEHONG BIOTECH CO., LTD. |
| Owner/operator | Guangzhou Hehong Biotech Co., Ltd. |
| Owner/operator number | 10093562 |
| FEI number | 3043639843 |
| Address | A zone, 2/F, Building A, Huazi Industrial Park, |
| City | Guangzhou Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | MQF, MQK |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 10–99 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