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Sign in to claim this brandTupelolife Services LLC
US
Last updated May 31, 2026
What Tupelolife Services LLC makes
Tupelolife Services LLC manufactures portable electronic sphygmomanometers designed for automatic inflation, suitable for measuring blood pressure on the arm or wrist. These devices are intended for home or clinical use to provide digital blood pressure readings.
The company’s products fall under FDA Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. Tupelolife Services LLC 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 Tupelolife Services LLC manufacture?
Tupelolife Services LLC specializes in portable electronic sphygmomanometers that automatically inflate to measure blood pressure. These devices are designed for use on either the arm or wrist, catering to both home and clinical environments. The focus is on providing digital blood pressure readings, making them convenient for monitoring.
Where is Tupelolife Services LLC based?
Tupelolife Services LLC is headquartered in the United States. The company’s location is relevant for understanding regulatory frameworks and compliance standards that may apply to its devices, particularly under U.S. medical device regulations.
Which regulatory registries or databases list Tupelolife Services LLC’s devices?
Tupelolife Services LLC’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.
How are Tupelolife Services LLC’s devices classified under U.S. regulations?
Tupelolife Services LLC’s devices fall under FDA Class II classification. This classification applies to devices that generally pose moderate risk and require special controls to ensure their safety and effectiveness, such as automatic-inflation electronic sphygmomanometers, which require performance testing and labeling requirements.
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
- 080844144
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| TupeloLife | TBP-002 | FDA UDI | Class II | Active |
| TupeloLife | TBP-001 | FDA UDI | Class II | Active |
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