RD Biomed (Changsha) Ltd.
Manufacturer and brand owner in Changsha, Hunan, China. 1 device type, 1 product catalogued.
RD Biomed (Changsha) Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Tubeless Analysis, Gastric Acidity. 1 of its products is catalogued under its own name. Its earliest product listing with the FDA dates from 2025.
1device type
1product
Registration
| Registered name | RD BIOMED (CHANGSHA) LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3043105517 |
| FEI number | 3043105517 |
| DUNS | 617582225 |
| Establishment type | Manufacturer |
Location
| City | Changsha |
|---|---|
| Province | Hunan |
| Address | Room 02, Unit 501, Building D7, Jinrong Enterprise Park, |
| Postal code | 410000 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Tubeless Analysis, Gastric Acidity | Class 1 | Pepfast lateral flow in vitro diagnostic medical device | 2025 | 1 |
Own-Brand Listings
| Product | Code | Catalogue numbers |
|---|---|---|
| Pepfast | JLL | 3 |
From the Company
Published by the company on its own website, not by the FDA.
| Main products | Peptest diagnostic device, Pharmaceutical development, Clinical trial services |
|---|---|
| Certifications | ISO 13485:2016 |
| Export markets | Global |
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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