Establishment registration
SHANDONG HENGFENG KERUI MEDICAL EQUIPMENT CO., LTD
FDA establishment registration 3031191035 · Qingdao City Shandong, CN
Key facts
| Registration number | 3031191035 |
|---|---|
| Establishment name | SHANDONG HENGFENG KERUI MEDICAL EQUIPMENT CO., LTD |
| Owner/operator | Shandong Hengfeng Kerui Medical Equipment Co., Ltd |
| Owner/operator number | 10090457 |
| FEI number | 3031191035 |
| Address | Room 102, 1st Floor, and Room 202, 2nd Floor, Building 19, Liandong U Valley Life and Health City |
| City | Qingdao City Shandong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DZC, DZN, EAX, ECS, EFS, EFW, EGD, EIS, EIY, EJL, EKM, EKN, EKQ, EKS, EMN, JEQ, JES, LCN, NDP |
| Device classes | 1 |
At a glance
- 10–99 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