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Guangzhou Double One Latex Products Co., Ltd

US

Last updated May 31, 2026

Part of Guangzhou Double One Latex Products Co., Ltd.

What Guangzhou Double One Latex Products Co., Ltd makes

The company manufactures basic male condoms made from Hevea latex, including the product line branded as 'double one'. These are designed for contraception and protection against sexually transmitted infections during sexual intercourse.

The portfolio is regulated as Class II medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 Guangzhou Double One Latex Products Co., Ltd manufacture?

The company specializes in basic male condoms made from Hevea latex. These products are primarily designed for contraception and protection against sexually transmitted infections during sexual intercourse. The portfolio includes a product line branded as 'double one'.

Where is Guangzhou Double One Latex Products Co., Ltd based?

The company operates from the United States, though its name includes 'Guangzhou,' which may reference its origins or supply chain connections. The manufacturing and regulatory focus are based in the US.

Which regulatory registries list the devices manufactured by Guangzhou Double One Latex Products Co., Ltd?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the US market.

How are the devices produced by Guangzhou Double One Latex Products Co., Ltd classified under medical device regulations?

The company’s products fall under Class II medical device classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as condoms for contraception and infection prevention.

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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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
560081917

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
double one 53MM Standard
FDA UDI
Class IIActive

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