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Sign in to claim this brandSAUVRE INTERNATIONAL, LTD.
US
Last updated May 24, 2026
What SAUVRE INTERNATIONAL, LTD. makes
The company manufactures single-use transcutaneous electrical stimulation electrodes and analgesic transcutaneous electrical nerve stimulation (TENS) systems, including branded devices like EASLIEF. These products are designed for pain management through electrical stimulation applied to the skin.
The portfolio consists of Class II medical devices, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 Sauvre International, Ltd. manufacture?
Sauvre International, Ltd. specializes in transcutaneous electrical stimulation products. Their portfolio includes single-use transcutaneous electrical stimulation electrodes and analgesic transcutaneous electrical nerve stimulation (TENS) systems, such as the branded device EASLIEF. These devices are designed to manage pain through controlled electrical stimulation applied to the skin.
Where is Sauvre International, Ltd. based?
Sauvre International, Ltd. is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.
Which regulatory registries list Sauvre International, Ltd.’s devices?
Sauvre International, Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class II medical devices, which include their transcutaneous electrical stimulation electrodes and TENS systems.
How are Sauvre International, Ltd.’s devices classified under medical device regulations?
Sauvre International, Ltd.’s devices fall under Class II classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
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
- 080557421
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Medical Science Products | 5090-FSD | FDA UDI | Class II | Active |
| Medical Science Products | COM-TENS | FDA UDI | Class II | Active |
| Easlief | ESLF50100 | FDA UDI | Class II | Active |
| Medical Science Products | 4040-SD | FDA UDI | Class II | Active |
| Easlief | ESLF4040 | FDA UDI | Class II | Active |
| Medical Science Products | 5050-FSD | FDA UDI | Class II | Active |
| RecoverPad | REPS2020 | FDA UDI | Class II | Unknown |
| Medical Science Products | 5050-WCSD | FDA UDI | Class II | Active |
| RecoverPad | REPSHS | FDA UDI | Class II | Unknown |
| RecoverPad | REPS2040 | FDA UDI | Class II | Unknown |
| RecoverPad | REPS4560 | FDA UDI | Class II | Unknown |
| Easlief | ESLF5050 | FDA UDI | Class II | Active |
| Medical Science Products | TS-1211 | FDA UDI | Class II | Active |
| Easlief | ESLF93150 | FDA UDI | Class II | Active |
| RecoverPad | REPS1515 | FDA UDI | Class II | Unknown |
| Medical Science Products | 110150-FSD | FDA UDI | Class II | Active |
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