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SEKI GLOBAL LLC

US

Last updated May 30, 2026

What SEKI GLOBAL LLC makes

SEKI GLOBAL LLC produces medical devices such as infrared patient thermometers, including the SANSHIELD. These devices are used to measure body temperature through the skin. The company's product portfolio includes devices that fall under the category of infrared patient thermometers.

The company's devices, including those classified as Class II, are listed in the FDA UDI registry. SEKI GLOBAL LLC is based in the US, where its devices are regulated. The company's products are subject to regulatory oversight, ensuring compliance with relevant standards and guidelines.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What type of medical devices does SEKI GLOBAL LLC produce?

SEKI GLOBAL LLC produces infrared patient thermometers designed to measure body temperature through the skin, such as the SANSHIELD device, which falls under the category of skin-contact infrared thermometers for patient use.

Where is SEKI GLOBAL LLC based?

SEKI GLOBAL LLC is based in the United States, as indicated in the company's country field, which specifies US as its location of operation and regulatory jurisdiction.

In which regulatory registry are SEKI GLOBAL LLC's devices listed?

SEKI GLOBAL LLC's devices are listed in the FDA UDI registry, which is the Unique Device Identification system managed by the U.S. Food and Drug Administration for tracking medical devices in the United States.

How are SEKI GLOBAL LLC's devices classified under regulatory standards?

SEKI GLOBAL LLC's devices, including the SANSHIELD infrared patient thermometer, are classified as Class II medical devices, indicating they require special controls to ensure safety and effectiveness but do not pose the highest risk level.

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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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
118095171

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Sanshield CK-T1502
FDA UDI
Class IIActive

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