Zhejiang Meihua Dingchang Pharmaceutical Co., Ltd.
Manufacturer and brand owner in Shaoxing, Zhejiang, China. 1 device type, 1 product catalogued.
Zhejiang Meihua Dingchang Pharmaceutical Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Splint, Intranasal Septal. 1 of its products is catalogued under its own name. Its earliest product listing with the FDA dates from 2019.
1device type
1product
Registration
| Status | Registered |
|---|---|
| Registration expires | 2026 |
| Registration number | 3016426830 |
| FEI number | 3016426830 |
| DUNS | 421293216 |
| Establishment type | Manufacturer |
Chinese Registration
| Chinese legal name | 浙江美华鼎昌医药科技有限公司 |
|---|---|
| Source | Qichacha company register |
Location
| City | Shaoxing |
|---|---|
| Province | Zhejiang |
| Address | Zhejiang Province,ShaoXing City,KeQiao District,XiHuan Road NO.586 |
| Postal code | 312000 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Splint, Intranasal Septal | Class 1 | Nasasponge | 2019 | 3 |
Own-Brand Listings
| Product | Code | Catalogue numbers |
|---|---|---|
| nasasponge | LYA | 1 |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 2011 |
|---|---|
| Factory area | 7,500 square meters |
| Main products | Solid sustained-release formulations, Biological peptide sustained-release formulations, High-end medical devices, Class I innovative drugs |
| Certifications | cGMP |
| Export markets | USA (subsidiary in New Jersey) |
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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