Establishment registration
ZHEJIANG LIDESEN MEDICAL INSTRUMENT CO., LTD
FDA establishment registration 3031184338 · Hangzhou Zhejiang, CN
Key facts
| Registration number | 3031184338 |
|---|---|
| Establishment name | ZHEJIANG LIDESEN MEDICAL INSTRUMENT CO., LTD |
| Owner/operator | Zhejiang Lidesen Medical Instrument Co., Ltd |
| Owner/operator number | 10090389 |
| FEI number | 3031184338 |
| Address | A-1931, Building 3, No. 228 Binkang Road, Xixing Street, Binjiang District |
| City | Hangzhou Zhejiang |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | BSJ, BSY, BTQ, BYF, BYG, BYY, CAT, CBH, CCQ, DYN, DZM, EFN, EIY, EXE, EYQ, EZQ, FAQ, FFG, FFH, FMA, FME, FMH, FNP, FNY, FOB, FOD, FON, FQL, FQM, FXP and 71 more |
| Device classes | 1, 2, N |
At a glance
- 100–999 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