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Sign in to claim this brandMERCATOR MEDICAL (THAILAND) LIMITED
US
Last updated September 17, 2026
Part of Mercator Medical (Thailand) Ltd.
What MERCATOR MEDICAL (THAILAND) LIMITED makes
Mercator Medical produces nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, including variants such as classic and blue-colored versions. These gloves are designed for medical examinations and procedures requiring barrier protection.
The company’s products are classified as Class I medical devices and are listed in the FDA’s Unique Device Identification (UDI) system. The manufacturer 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 Mercator Medical (Thailand) Limited manufacture?
Mercator Medical (Thailand) Limited specializes in producing nitrile examination and treatment gloves. These gloves are designed for medical examinations and procedures, providing a barrier against contamination. The company’s products are specifically non-powdered and non-antimicrobial, including variations like classic and blue-colored versions.
Where is Mercator Medical (Thailand) Limited based?
The company is based in the United States. While the name includes 'Thailand,' the operational headquarters and manufacturing are located in the US, as indicated by the provided details.
Which regulatory registries list Mercator Medical’s devices?
Mercator Medical’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry helps track and identify medical devices authorized for use in the US, ensuring traceability and compliance.
How are Mercator Medical’s devices classified under regulatory standards?
Mercator Medical’s nitrile examination and treatment gloves fall under Class I medical device classification. Class I devices are generally considered low-risk and typically do not require pre-market approval, but they must still meet regulatory requirements for safety and performance.
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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- 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
- 671647476
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| nitrylex classic+ | RD30246902_0001 | FDA UDI | Class I | Active |
| nitrylex classic blue | RD30019905_0001 | FDA UDI | Class I | Active |
| nitrylex classic+ | RD30246901_0001 | FDA UDI | Class I | Active |
| nitrylex classic blue | RD30019901_0001 | FDA UDI | Class I | Active |
| nitrylex classic blue | RD30019904_0001 | FDA UDI | Class I | Active |
| nitrylex classic blue | RD30019903_0001 | FDA UDI | Class I | Active |
| nitrylex classic blue | RD30019902_0001 | FDA UDI | Class I | Active |
| nitrylex classic+ | RD30246904_0001 | FDA UDI | Class I | Active |
| nitrylex classic+ | RD30246905_0001 | FDA UDI | Class I | Active |
| nitrylex classic+ | RD30246903_0001 | FDA UDI | Class I | Active |
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