Identity
- Trade Name
- ProActive Alevia 2 in 1 TENS FDA UDI
- Generic Name
- Analgesic transcutaneous electrical nerve stimulation system FDA UDI
- Device Name
- The TENS 2-in-1 Physiotherapy Alevia™ by ProActive™ is a 2-in-1 (TENS and EMS) device that gives you the ability to fully customize treatment options or choose one of the 18 pre-set programs. It has a large, easy-to-read LCD and includes all accessories. The Alevia™ comes complete with 4 self-adhesive, pre-gelled and reusable electrodes, one rechargeable battery with USB Cable, lead wires, instructions and a storage bag. ProActive™ offers a complete line of physiotherapy devices, clinically proven to relieve pain without drugs, including a full line-up of electrodes. The Alevia™ Dual channel TENS Electro-Stimulator relieves pain in 2 ways: TENS (Transcutaneous Nerve Stimulation) stimulates or numbs nerves EMS (Electrical Muscle Stimulation) prevents atrophy FDA UDI
- Model / Reference
- 715-425 FDA UDI
- Description
- The TENS 2-in-1 Physiotherapy Alevia™ by ProActive™ is a 2-in-1 (TENS and EMS) device that gives you the ability to fully customize treatment options or choose one of the 18 pre-set programs. It has a large, easy-to-read LCD and includes all accessories. The Alevia™ comes complete with 4 self-adhesive, pre-gelled and reusable electrodes, one rechargeable battery with USB Cable, lead wires, instructions and a storage bag. ProActive™ offers a complete line of physiotherapy devices, clinically proven to relieve pain without drugs, including a full line-up of electrodes. The Alevia™ Dual channel TENS Electro-Stimulator relieves pain in 2 ways: TENS (Transcutaneous Nerve Stimulation) stimulates or numbs nerves EMS (Electrical Muscle Stimulation) prevents atrophy FDA UDI
Identifiers
- Catalog Number
- 715-425 FDA UDI
- Primary DI / UDI-DI
- 00775757154251 FDA UDI
- FDA Product Code
- NGX FDA UDI
- GMDN Term
- Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5850 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Analgesic transcutaneous electrical nerve stimulation system
ProActive Alevia 2 in 1 TENS by A.M.G. Médicale Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- A.M.G. Médicale Inc
Sources (1)
- FDA UDI 6895a91f-5d72-47e6-a22e-9a1d7587ff00 34 fields · synced May 30, 2026