Establishment registration
GUANGDONG TIDAKANG MEDICAL TECHNOLOGY CO., LTD
FDA establishment registration 3015335956 · ZhongShan City Guangdong, CN
Key facts
| Registration number | 3015335956 |
|---|---|
| Establishment name | GUANGDONG TIDAKANG MEDICAL TECHNOLOGY CO., LTD |
| Owner/operator | GuangDong TiDaKang Medical Technology Co., Ltd |
| Owner/operator number | 10060082 |
| FEI number | 3015335956 |
| Address | First Floor Area A, Second Floor Area A, Third Floor Area A, Fourth Floor Area A, Fifth Floor Area A |
| City | ZhongShan City Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | EMX, FMP, FOK, FXN, HMP, KGX, KMK, MHW, NAC, NAD, NAE, PFP |
| 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