Zhejiang LuDe Technology Development Co., Ltd.
Registered establishment in Wenzhou, Zhejiang, China. 2 device types, 1 clearance.
Zhejiang LuDe Technology Development Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Blood Pressure Cuff, Stethoscope, Manual. Its earliest product listing with the FDA dates from 2024.
2device types registered with the FDA
1510(k) clearance
Registration
| Status | Registered |
|---|---|
| Registration expires | 2026 |
| Registration number | 3031192529 |
| FEI number | 3031192529 |
| Establishment type | Manufacturer |
Chinese Registration
| Chinese legal name | 浙江鹿得科技发展有限公司 |
|---|---|
| Source | Qichacha company register |
Location
| City | Wenzhou |
|---|---|
| Province | Zhejiang |
| Address | NO. 298 Jichang North Road, Longwan District |
| Postal code | 325024 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Blood Pressure Cuff | Class 2 | Aneroid sphygmomanometer QL-20, QL-50, QL-201 (20A, 50A, 201C1) | 2024 | 50 |
| Stethoscope, Manual | Class 1 | Aneroid sphygmomanometer QL-20, QL-50, QL-201 (20A, 50A, 201C1) | 2024 | 64 |
Clearances
| Clearance | Decision date | Product code | Route | Held by |
|---|---|---|---|---|
| K221857 | 2022-10-13 | DXQ | Traditional | This company |
From the Company
Published by the company on its own website, not by the FDA.
| Main products | Stethoscopes, Respiratory monitoring devices, Cardiovascular monitoring devices |
|---|---|
| Export markets | Global distribution network |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
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