Establishment registration
CANGZHOU LANKANG MEDICAL INSTRUMENTS DEVELOPING CO., LTD.
FDA establishment registration 3008346537 · Cangzhou Hebei, CN
Key facts
| Registration number | 3008346537 |
|---|---|
| Establishment name | CANGZHOU LANKANG MEDICAL INSTRUMENTS DEVELOPING CO., LTD. |
| Owner/operator | Cangzhou Lankang Medical Instruments Developing Co., Ltd. |
| Owner/operator number | 10051715 |
| FEI number | 3008346537 |
| Address | ROOM 101, BUILDING 16, No. 2 JINGBA ROAD, CANGZHOU ECONOMIC DEVELOPMENT ZONE |
| City | Cangzhou Hebei |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DYN, DZN, EAX, EBL, ECB, EFT, EFW, EGD, EGZ, EHY, EHZ, EID, EIF, EIL, EIX, EJL, EJQ, EKS, EMG, FRK, FSM, GAF, GED, IWS, JEP, JES, JET, KHR, KXF, KYW and 10 more |
| 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