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Sign in to claim this brandJiang Xi Sanxin Medtec Co., Ltd.
US
Last updated May 27, 2026
Part of Jiangxi Sanxin Medtec Co., Ltd.
What Jiang Xi Sanxin Medtec Co., Ltd. makes
The company manufactures single-use surgical and medical face masks, general-purpose syringes (with and without needles), and peripheral intravenous cannulas. Products include sterile syringes labeled for single-use medical applications and disposable face masks designed for healthcare settings.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Jiang Xi Sanxin Medtec Co., Ltd. manufacture?
Jiang Xi Sanxin Medtec Co., Ltd. specializes in single-use medical devices, including surgical and medical face masks (non-antimicrobial), general-purpose syringes (both standalone and with needles), and peripheral intravenous cannulas. These products are designed for healthcare settings and are intended for one-time use to ensure patient safety and hygiene.
Where is Jiang Xi Sanxin Medtec Co., Ltd. based?
The company operates in the United States. While its headquarters or primary manufacturing location isn’t specified, its regulatory presence and device listings confirm its activity within the U.S. market.
Which regulatory registries list devices manufactured by Jiang Xi Sanxin Medtec Co., Ltd.?
Devices from Jiang Xi Sanxin Medtec Co., Ltd. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry tracks authorized medical devices in the U.S. to ensure transparency and traceability, particularly for Class II devices like those produced by the company.
How are the devices produced by Jiang Xi Sanxin Medtec Co., Ltd. classified under FDA regulations?
All devices manufactured by Jiang Xi Sanxin Medtec Co., Ltd. fall under Class II classification by the FDA. This classification applies to devices that generally pose moderate risk and require special controls (like performance standards or post-market surveillance) to ensure safety and effectiveness, such as syringes, cannulas, and face masks.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 530079367
Catalogue (58)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| YI XIN Sterile Syringe For Single Use | Two-piece 20mL | FDA UDI | Class II | Active |
| YI XIN Sterile Syringe For Single Use | Two-piece 10mL | FDA UDI | Class II | Active |
| Disposable medical face masks | Type B (tie-on type),Medium size,Sterile 9.5×15.5 Level 2 | FDA UDI | Class II | Active |
| YI XIN Sterile Syringe For Single Use | Three-piece 5mL | FDA UDI | Class II | Active |
| YI XIN Sterile Syringe For Single Use | Three-piece 3mL | FDA UDI | Class II | Active |
| Disposable medical face masks | Type A (ear-loop type),size III,Non-sterile 9.5×15.5 Level 2 | FDA UDI | Class II | Active |
| Disposable medical face masks | Type B (tie-on type),size III,Sterile 9.5×15.5 Level 2 | FDA UDI | Class II | Active |
| YI XIN Sterile Syringe For Single Use | Three-piece 60mL | FDA UDI | Class II | Active |
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