Establishment registration
HENAN BAISTRA MEDICAL DEVICES LIMITED
FDA establishment registration 3023443842 · Zhengzhou Henan, CN
Key facts
| Registration number | 3023443842 |
|---|---|
| Establishment name | HENAN BAISTRA MEDICAL DEVICES LIMITED |
| Owner/operator | HENAN BAISTRA MEDICAL DEVICES LIMITED |
| Owner/operator number | 10085746 |
| FEI number | 3023443842 |
| Address | 80 DIANCHANG RD, BUILDING 162, FLOOR 20, SUITE 61, HI-TECH INDUSTRIES DEVELOPMENT, |
| City | Zhengzhou Henan |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | BZN, DYN, DZD, DZN, EAX, EAZ, ECI, ECN, EFH, EGD, EHL, EHM, EHY, EID, EIF, EIY, EJF, EJL, EJQ, EJR, EKM, EKS, FRK, FSM, GES, HJH, INN, KMT, LXH, MDM and 4 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