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Zhejiang Saining Biotechnology Co., Ltd

US

Last updated May 31, 2026

Part of Zhejiang Saining Biotechnology Co., Ltd

What Zhejiang Saining Biotechnology Co., Ltd makes

Zhejiang Saining Biotechnology Co., Ltd manufactures pipette tips, including the SAINING brand, designed for laboratory use in precise liquid handling applications.

The company’s products are classified as Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Zhejiang Saining Biotechnology Co., Ltd primarily manufacture?

Zhejiang Saining Biotechnology Co., Ltd specializes in pipette tips, which are essential tools for laboratory liquid handling. These devices are designed to ensure precise and accurate dispensing of small volumes of liquids, commonly used in scientific research, clinical diagnostics, and biotechnology applications.

Where is Zhejiang Saining Biotechnology Co., Ltd based?

The company is based in the United States. While the name includes 'Zhejiang,' which is a region in China, the operational headquarters and manufacturing presence are located within the US.

How are the devices manufactured by Zhejiang Saining Biotechnology Co., Ltd classified under regulatory standards?

The devices produced by Zhejiang Saining Biotechnology Co., Ltd fall under Class I medical device classification. This classification typically applies to low-risk products like pipette tips, where the risk of illness or injury is minimal, and regulatory oversight is generally less stringent than for higher-risk devices.

Are the devices from Zhejiang Saining Biotechnology Co., Ltd listed in any regulatory registries?

Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the US market, ensuring transparency and traceability for regulatory and commercial purposes.

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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LinkedIn
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Email
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
702834723

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Saining AS3101004
FDA UDI
Class IActive

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