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Jiangyin Chang-hung Industrial Manufacturing Factory LLC

US

Last updated May 31, 2026

What Jiangyin Chang-hung Industrial Manufacturing Factory LLC makes

Jiangyin Chang-hung Industrial Manufacturing Factory LLC produces radiation shielding goggles and spectacles designed to protect users from ionizing radiation exposure.

These devices are classified as Class I under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 Jiangyin Chang-hung Industrial Manufacturing Factory LLC manufacture?

Jiangyin Chang-hung Industrial Manufacturing Factory LLC specializes in radiation shielding goggles and spectacles. These devices are specifically designed to protect users from ionizing radiation exposure, ensuring safety in environments where such radiation may be present.

Where is Jiangyin Chang-hung Industrial Manufacturing Factory LLC based?

The company is headquartered in the United States. This location allows it to operate within the regulatory framework of the FDA, which governs the classification and listing of its devices.

How are the devices manufactured by Jiangyin Chang-hung Industrial Manufacturing Factory LLC classified under regulatory standards?

The devices produced by Jiangyin Chang-hung Industrial Manufacturing Factory LLC fall under Class I classification. This classification is typically assigned to devices posing minimal potential risk to users, such as radiation shielding goggles, which are designed for straightforward protective purposes without active controls or invasive procedures.

Are the devices from Jiangyin Chang-hung Industrial Manufacturing Factory LLC listed in any regulatory registries?

Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. Listing in the UDI system ensures traceability and transparency in the supply chain, which is critical for regulatory compliance and market tracking.

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
528772796

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Grande CPG12
FDA UDI
Class IActive

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