Identity
- Trade Name
- WiTouch FDA UDI
- Generic Name
- Analgesic transcutaneous electrical nerve stimulation system FDA UDI
- Device Name
- WiTouch brand over the counter transcutaneous electrical nerve simulator for analgesic pain relief in the lower back FDA UDI
- Model / Reference
- 11.1510 FDA UDI
- Description
- WiTouch brand over the counter transcutaneous electrical nerve simulator for analgesic pain relief in the lower back FDA UDI
Identifiers
- Catalog Number
- 11.1510 FDA UDI
- Primary DI / UDI-DI
- 00853096004014 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
- Not 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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Height — 90 Millimeter FDA UDIWidth — 191 Millimeter FDA UDIOuter Diameter — 18 Millimeter FDA UDI
WiTouch by Hollywog, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Hollywog, LLC
Sources (1)
- FDA UDI 75829d70-4362-41c9-bd2e-79ca3172b977 38 fields · synced May 30, 2026