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Sign in to claim this brandAnhui Kangda Medical Products Co., Ltd.
US
Last updated May 23, 2026
What Anhui Kangda Medical Products Co., Ltd. makes
The company manufactures single-use syringes and needles, including general-purpose and dental variants, as well as invasive blood collection and intravenous administration sets. These products are designed for medical procedures requiring precise fluid delivery or withdrawal, including blood draws and intravenous therapies.
The portfolio includes devices classified as Class I and Class II under regulatory frameworks, with submissions recorded in the FDA’s 510(k) and UDI registries. The company is based 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 Anhui Kangda Medical Products Co., Ltd. primarily manufacture?
Anhui Kangda Medical Products Co., Ltd. specializes in single-use medical devices, including general-purpose syringes and needles, dental syringe needles, blood collection sets, and basic intravenous administration sets. These products are designed for tasks like blood collection, intravenous therapies, and precise fluid administration in clinical settings.
Where is Anhui Kangda Medical Products Co., Ltd. based?
The company is based in the United States. While the name suggests an origin in China, the regulatory submissions and listings indicate its operational presence in the US market.
Which regulatory registries list devices manufactured by Anhui Kangda Medical Products Co., Ltd.?
Devices from Anhui Kangda Medical Products Co., Ltd. appear in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) database. These registries track submissions and classifications for medical devices in the US market.
How are the devices manufactured by Anhui Kangda Medical Products Co., Ltd. classified under regulatory frameworks?
The company’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and may require less stringent controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness.
Why do some of Anhui Kangda Medical Products Co., Ltd.’s devices appear repeatedly in listings?
The repeated appearance of the same device name (e.g., BAIXIN) in listings likely reflects multiple submissions or variations of the same product line, such as different sizes, packaging, or slight design modifications. Each submission may correspond to a distinct model or regulatory filing for market authorization.
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
- 529827552
Catalogue (59)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| baixin | 27GDN | FDA UDI | Class I | Active |
| Baixin | KD201 | FDA UDI | Class II | Active |
| Baixin | 2ML23GSLIP | FDA UDI | Class II | Active |
| Baixin | 25GSVS | FDA UDI | Class I | Active |
| Baixin | 5MLLL | FDA UDI | Class II | Active |
| Baixin | 50ML21GLOCK | FDA UDI | Class II | Active |
| Baixin | 3MLLL2515 | FDA UDI | Class II | Active |
| Baixin Intravascular Administration Set | K083687 | FDA 510(k) | Class II | Active |
| Baixin Disposable Syringe, Multiple Sizes | K083686 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Anhui Kangda Medical Products Co., Ltd. Tianchang City Anhui · CN FEI 3003310007