Identity
- Trade Name
- Pain Aide FDA UDI
- Generic Name
- Analgesic transcutaneous electrical nerve stimulation system FDA UDI
- Device Name
- Pain Aide is a TENS device which is commonly used to provide relief from pain associated with sore or aching muscles of the lower back, arms, or legs due to strain from exercise or normal household and work activities. It has four preset programs specially designed to alleviate pain in different parts of the body. Pain Aide is designed to be easy to use, but has professional grade features like small 1 mA intensity steps, open-circuit detection with cutout, automatic keypad locking, and back-lit display. It uses standard AA batteries and self-adhesive electrode pads. Garment glove and sock electrodes are available as optional extras. FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- Pain Aide is a TENS device which is commonly used to provide relief from pain associated with sore or aching muscles of the lower back, arms, or legs due to strain from exercise or normal household and work activities. It has four preset programs specially designed to alleviate pain in different parts of the body. Pain Aide is designed to be easy to use, but has professional grade features like small 1 mA intensity steps, open-circuit detection with cutout, automatic keypad locking, and back-lit display. It uses standard AA batteries and self-adhesive electrode pads. Garment glove and sock electrodes are available as optional extras. FDA UDI
Identifiers
- Catalog Number
- K-PA FDA UDI
- Primary DI / UDI-DI
- 05033435132232 FDA UDI
- FDA Product Code
- NUH FDA UDI
- GMDN Term
- Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5890 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Analgesic transcutaneous electrical nerve stimulation system
Pain Aide by Tenscare Limited — 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
- Tenscare Limited
Sources (1)
- FDA UDI 4bf39cb9-f214-486e-83d6-f2581feb6fc7 36 fields · synced Jun 6, 2026