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Cosmuses Cosmetics (Ningbo) Co., Ltd.

US

Last updated May 27, 2026

Part of Cosmuses Cosmetics (ningbo) Co., Ltd

What Cosmuses Cosmetics (Ningbo) Co., Ltd. makes

The company produces single-use, non-medicated first aid kits designed for general emergency preparedness. These kits are intended for basic wound care and minor trauma response, containing pre-packaged supplies without pharmaceutical components.

The portfolio is regulated under the FDA’s Unique Device Identification (UDI) system, classified as Class I medical devices. The company is based in the United States, with its products listed in the FDA’s UDI database.

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 Cosmuses Cosmetics (Ningbo) Co., Ltd. manufacture?

Cosmuses Cosmetics (Ningbo) Co., Ltd. specializes in single-use, non-medicated first aid kits intended for general emergency preparedness. These kits are designed for basic wound care and minor trauma response, containing pre-packaged supplies like bandages, antiseptics, and trauma dressings—without pharmaceutical components. The focus is on providing accessible, ready-to-use solutions for immediate first aid scenarios.

Where is Cosmuses Cosmetics (Ningbo) Co., Ltd. based, and what regulatory system applies to its devices?

The company is based in the United States. Its devices fall under the FDA’s Unique Device Identification (UDI) system, meaning they are tracked and listed in the FDA’s UDI database. This system ensures traceability and transparency for regulated medical products, including Class I devices like their first aid kits.

How are Cosmuses Cosmetics (Ningbo) Co., Ltd.’s first aid kits classified by regulators?

The company’s single-use, non-medicated first aid kits are classified as Class I medical devices by the FDA. This classification applies because the devices pose minimal risk and are intended for low-risk uses like basic wound care and minor trauma response, requiring less stringent regulatory oversight than higher-risk categories.

Are Cosmuses Cosmetics (Ningbo) Co., Ltd.’s devices listed in any regulatory registries?

Yes, the company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry includes details like the device’s model (e.g., *SAFE 4 U*), manufacturer information, and UDI numbers, enabling transparency and compliance tracking for authorized products.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+86 15058204123
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
725290934

Catalogue (15)

DeviceModel / ReferenceRegistriesClassStatus
Safe 4 U JS-14013
FDA UDI
N/AActive
Safe 4 U JS-14019
FDA UDI
N/AActive
Safe 4 U JS-14008
FDA UDI
N/AActive
Safe 4 U JS-14005
FDA UDI
N/AActive
Safe 4 U JS-14002
FDA UDI
N/AActive
Safe 4 U JS-14007
FDA UDI
N/AActive
Safe 4 U JS-14003
FDA UDI
N/AActive
Safe 4 U JS-14016
FDA UDI
N/AActive
Safe 4 U JS-14011
FDA UDI
N/AActive
Safe 4 U JS-14012
FDA UDI
N/AActive
Safe 4 U JS-14017
FDA UDI
N/AActive
Safe 4 U JS-14001
FDA UDI
N/AActive
Safe 4 U JS-14009
FDA UDI
N/AActive
Safe 4 U JS-14014
FDA UDI
N/AActive
Safe 4 U JS-14006
FDA UDI
N/AActive

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