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Sign in to claim this brandSEEMTRAMED LLC
US
Last updated May 30, 2026
What SEEMTRAMED LLC makes
Seemtramed LLC manufactures portable electronic blood pressure monitors designed for arm or wrist use, which automatically inflate to measure readings, and infrared thermometers that measure temperature via the ear or forehead. These devices are intended for home or clinical use to track vital signs like blood pressure and body temperature.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The devices are intended for commercial distribution 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 Seemtramed LLC manufacture?
Seemtramed LLC produces two primary types of medical devices: automatic-inflation electronic sphygmomanometers for arm or wrist use, which measure blood pressure, and infrared thermometers designed to take readings from the ear or forehead. These devices are intended for both home and clinical environments to help monitor vital signs like blood pressure and body temperature.
Where is Seemtramed LLC based, and where are its devices primarily intended for use?
Seemtramed LLC is based in the United States. The company’s devices are specifically intended for commercial distribution within the U.S., though their design and functionality may also be relevant in other markets depending on local regulations.
Which regulatory registries or databases list Seemtramed LLC’s devices?
Seemtramed LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorised for commercial distribution in the U.S., ensuring transparency and traceability.
How are Seemtramed LLC’s devices classified under FDA regulations?
Seemtramed LLC’s devices fall under Class II classification according to FDA regulations. This classification applies to devices that generally pose moderate risk and require special controls—such as performance standards or post-market surveillance—to ensure their safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- [email protected]
- Phone
- 917-720-2575
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 117025040
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SeemtraMed Blood Pressure Monitor | SBPM-1585-S | FDA UDI | Class II | Active |
| SeemtraMed Infrared Ear/Forehead Thermometer | PG-IRT1603 | FDA UDI | Class II | Active |
| SeemtraMed Infrared Thermometer | EF 100A | FDA UDI | Class II | Unknown |
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