Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

SEEMTRAMED 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
—
LinkedIn
—
Facebook
—
Phone
917-720-2575
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
117025040

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
SeemtraMed Blood Pressure Monitor SBPM-1585-S
FDA UDI
Class IIActive
SeemtraMed Infrared Ear/Forehead Thermometer PG-IRT1603
FDA UDI
Class IIActive
SeemtraMed Infrared Thermometer EF 100A
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.