Hantech (Ningbo) Medical Technology Co., Ltd.
Registered establishment in Ningbo, Zhejiang, China. 3 device types.
Hantech (Ningbo) Medical Technology Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Syringe, Piston, Saline, Vascular Access Flush and 1 other device type. Its earliest product listing with the FDA dates from 2026.
Registration
| Registered name | HANTECH (NINGBO) MEDICAL TECHNOLOGY CO., LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3043709866 |
| FEI number | 3043709866 |
| Establishment type | Contract manufacturer, Manufacturer |
Location
| City | Ningbo |
|---|---|
| Province | Zhejiang |
| Address | No. 836 Yuhai East Road, Qianwan New District, Ningbo, Zhejiang Province, China |
| Postal code | 315336 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | Class 2 | Disposable Medical Safety Hypodermic Needle | 2026 | 71 |
| Saline, Vascular Access Flush | Class 2 | Pre-filled 0.9% Normal Saline Flush Syringes | 2026 | 10 |
| Syringe, Piston | Class 2 | Insulin Syringe | 2026 | 60 |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 2004 |
|---|---|
| Employees | 201-500 |
| Factory area | 16,882 m² |
| Main products | disposable medical devices, PTCA, alimentary tract devices, respiratory devices, urology devices |
| Certifications | FDA, ISO 13485, CE, GMP |
| OEM and ODM | Offered |
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.
The manufacturer named here can complete this record.