Is this your brand? Sign in to claim ownership.
Sign in to claim this brandGuangzhou Double One Latex Products Co., Ltd
US
Last updated May 31, 2026
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
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 560081917
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| double one | 53MM Standard | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.