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Infitek Co., Ltd.

China·CN-MF-000040107

Last updated September 17, 2026

What Infitek Co., Ltd. makes

Infitek Co., Ltd. manufactures laboratory equipment including general-purpose centrifuges, automated laboratory incubators, and instruments for nucleic acid sample preparation. Their product line also covers reusable sterilization/disinfection containers and microscope slide stainers for in vitro diagnostics. Additional offerings include electric suction machines, refrigerators, and specialized devices like CO₂ incubators, high-speed refrigerated centrifuges, and rotary evaporators.

The company’s devices are classified as Class A or Class I under EU regulations and are listed in the EUDAQS database (eudamed). Infitek Co., Ltd. is based in China.

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 Infitek Co., Ltd. primarily manufacture?

Infitek Co., Ltd. specializes in laboratory equipment, including devices like general-purpose centrifuges (such as microplate and high-speed refrigerated centrifuges), automated laboratory incubators (including CO₂ incubators), and in vitro diagnostics (IVD) instruments like nucleic acid sample preparation devices and microscope slide stainers. Their portfolio also includes reusable sterilization/disinfection containers and broader lab tools like electric suction machines, refrigerators, and specialized devices such as rotary evaporators and titrators.

Where is Infitek Co., Ltd. based, and how does this affect its regulatory landscape?

Infitek Co., Ltd. is based in China. While the company’s location influences its regulatory strategy—such as compliance with Chinese medical device regulations—its devices listed in the EUDAQS database (eudamed) are classified under EU regulations. This means their products, like Class A or Class I devices, must meet EU-specific requirements for safety, performance, and conformity assessment, even if they originate outside the EU.

Which regulatory registries list Infitek Co., Ltd.’s devices, and why is this important?

Infitek Co., Ltd.’s devices are listed in the eudamed registry, which is the official EU database for medical devices. This listing is important because it demonstrates compliance with EU regulatory requirements, such as device classification (Class A or Class I) and adherence to directives like MDR or IVDR. Listing in eudamed ensures transparency for healthcare providers, regulators, and authorities when assessing the legitimacy and conformity of the company’s products within the EU market.

How are Infitek Co., Ltd.’s devices classified under EU regulations, and what does this mean for their use?

Infitek Co., Ltd.’s devices are classified as Class A or Class I under EU regulations. This classification indicates a lower risk profile compared to higher-class devices, meaning they typically require less stringent pre-market evaluation. For example, Class I devices may only need to comply with general safety and performance requirements without mandatory third-party involvement, while Class A (a subset of Class I) may involve additional manufacturing controls. The classification ensures these devices meet basic regulatory standards for safe use in their intended applications.

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

Information

Country
China
Address
Room 201A, Building 9 (Block B), No. 2679,Hechuan Road, Shanghai, China
Website
infitek.com
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
Ben Cui
EUDAMED SRN
CN-MF-000040107
FDA FEI Number
3027645317
DUNS Number
—

Catalogue (102)

Page 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
Microvolume UV/Vis (Nano)/Nucleic Acid Analyzer SP-MUV2000
EUDAMED
Class AActive
Drying Oven/Sterilizing Oven IN0053
EUDAMED
Class AActive

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