Establishment registration
GUILIN REFINE MEDICAL INSTRUMENT CO., LTD.
FDA establishment registration 3016075921 · Guilin Guangxi, CN
Key facts
| Registration number | 3016075921 |
|---|---|
| Establishment name | GUILIN REFINE MEDICAL INSTRUMENT CO., LTD. |
| Owner/operator | Guilin Refine Medical Instrument Co., LTD. |
| Owner/operator number | 10064688 |
| FEI number | 3016075921 |
| Address | NO.8-3, Information Industrial Park, High-Tech Zone, Qixing District |
| City | Guilin Guangxi |
| Country | CN |
| Establishment types | Contract manufacturer, Foreign exporter |
| Registration valid through | 2026 |
| Product codes listed | EBR, EBZ, EHD, EJR, EKR, ELC, JET |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 1–9 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