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Tianjin Huashang Medical Equipment Co.,Ltd.

China·CN-MF-000015649

Last updated September 17, 2026

What Tianjin Huashang Medical Equipment Co.,Ltd. makes

Tianjin Huashang Medical Equipment Co., Ltd. manufactures single-use lancets designed for blood glucose monitoring and other capillary blood sampling procedures. These devices are intended for repeated skin punctures in clinical, home healthcare, and diabetic management settings, ensuring minimal discomfort and controlled bleeding.

The company’s lancets are classified as Class IIa medical devices under EU regulations and are listed in the EU’s eudamed registry. The devices are intended for use within the European market, adhering to applicable conformity assessment procedures for this classification.

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 Tianjin Huashang Medical Equipment Co., Ltd. manufacture?

Tianjin Huashang Medical Equipment Co., Ltd. specializes in single-use lancets. These devices are primarily designed for blood glucose monitoring and capillary blood sampling, commonly used in clinical settings, home healthcare, and diabetic management. The lancets are intended for repeated skin punctures, ensuring minimal patient discomfort and controlled bleeding.

Where is Tianjin Huashang Medical Equipment Co., Ltd. based?

The company is based in China (CN). While its location influences its regulatory and manufacturing operations, the specific details of its facilities or regional focus are not provided in the available data.

Which regulatory registries list the devices manufactured by Tianjin Huashang Medical Equipment Co., Ltd.?

The company’s lancets are listed in the eudamed registry, which is the European database for medical devices. This registry is used to track devices that comply with EU Medical Device Regulations (MDR) or the previous Medical Device Directives (MDD). Listing in eudamed confirms the device’s conformity assessment and market surveillance requirements under EU regulations.

How are the devices manufactured by Tianjin Huashang Medical Equipment Co., Ltd. classified under EU regulations?

The lancets produced by Tianjin Huashang Medical Equipment Co., Ltd. are classified as Class IIa medical devices under EU regulations. This classification is determined based on their intended use—repeated skin punctures for blood sampling—which presents moderate risks. Class IIa devices require a conformity assessment procedure, typically involving a Notified Body review, to ensure safety and performance before market placement.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
China
Address
East 1F,C-10Building, No.80 HaiYun Street,TEDA, Tianjin, Tianjin, China
LinkedIn
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Facebook
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Phone
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PRRC Contact
Feng Yanhong
EUDAMED SRN
CN-MF-000015649
FDA FEI Number
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DUNS Number
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Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
Lancets 28G
EUDAMED
Class IIaActive
Lancets 30G
EUDAMED
Class IIaActive
Lancets 25G
EUDAMED
Class IIaActive
Lancets 26G
EUDAMED
Class IIaActive
Lancets 23G
EUDAMED
Class IIaActive

Related Companies

Authorised Representatives

Importers

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Notified Bodies

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Authorities

Not available yet.