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Anhui 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
—
Website
—
LinkedIn
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Facebook
—
Email
—
Phone
—
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 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Baixin 5ML22GLOCK
FDA UDI
Class IIActive
Baixin KD204
FDA UDI
Class IIActive
Baixin 3ML23GSLIP
FDA UDI
Class IIActive
Baixin 1MLLS251
FDA UDI
Class IIActive
Baixin 24GSVS
FDA UDI
Class IActive
Baixin 1MLLS2515
FDA UDI
Class IIActive
Baixin KD210
FDA UDI
Class IIActive
Baixin 1MLLL231
FDA UDI
Class IIActive
Baixin 3MLLS2315
FDA UDI
Class IIActive
Baixin KD207
FDA UDI
Class IIActive
Baixin 3MLLL2315
FDA UDI
Class IIActive
Baixin KD212
FDA UDI
Class IIActive
baixin 30GDN
FDA UDI
Class IActive
Baixin 1MLLL2315
FDA UDI
Class IIActive
Baixin 18GSVS
FDA UDI
Class IActive
Baixin 5MLLL251
FDA UDI
Class IIActive
Baixin KD206
FDA UDI
Class IIActive
Baixin 3MLLL231
FDA UDI
Class IIActive
Baixin 60ML21GSLIP
FDA UDI
Class IIActive
Baixin 1MLLS2315
FDA UDI
Class IIActive
Baixin 21GSVS
FDA UDI
Class IActive
Baixin 1MLLL2515
FDA UDI
Class IIActive
Baixin 20ML21GSLIP
FDA UDI
Class IIActive
Baixin 1MLLL
FDA UDI
Class IIActive
Aquilavie Healthcare AQINJ-LS01-2525
FDA UDI
Class IIActive
Baixin 3MLLL251
FDA UDI
Class IIActive
Baixin 5MLLL231
FDA UDI
Class IIActive
Baixin 1MLLL251
FDA UDI
Class IIActive
Baixin 1ML27GSLIP
FDA UDI
Class IIActive
Baixin 3MLLS2515
FDA UDI
Class IIActive
Aquilavie J10003
FDA UDI
Class IIUnknown
Baixin 19GSVS
FDA UDI
Class IActive
Baixin 20ML21GLOCK
FDA UDI
Class IIActive
Baixin 10ML21GLOCK
FDA UDI
Class IIActive
Baixin 23GSVS
FDA UDI
Class IActive
Baixin 26GSVS
FDA UDI
Class IActive
Baixin 60ML21GLOCK
FDA UDI
Class IIActive
Baixin 22GSVS
FDA UDI
Class IActive
Baixin KD209
FDA UDI
Class IIActive
Baixin 50ML21GSLIP
FDA UDI
Class IIActive
Baixin 3ML23GLOCK
FDA UDI
Class IIActive
Baixin 27GSVS
FDA UDI
Class IActive
Baixin 1MLLS231
FDA UDI
Class IIActive
Baixin 3MLLS231
FDA UDI
Class IIActive
Baixin 3MLLL
FDA UDI
Class IIActive
Baixin 20GSVS
FDA UDI
Class IActive
Baixin 3MLLS251
FDA UDI
Class IIActive
Baixin 5ML22GSLIP
FDA UDI
Class IIActive
Baixin 10ML21GSLIP
FDA UDI
Class IIActive
Baixin 2ML23GLOCK
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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