Identity
- Trade Name
- e-vive NMES Electrode Set with Hook Backings FDA UDI
- Generic Name
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
- Device Name
- e-vive NMES Electrode Set with Hook Backings FDA UDI
- Model / Reference
- CY-1000-019 FDA UDI
- Description
- e-vive NMES Electrode Set with Hook Backings FDA UDI
Identifiers
- Catalog Number
- CY-1000-019 FDA UDI
- Primary DI / UDI-DI
- 00854816006721 FDA UDI
- FDA Product Code
- KQX FDA UDIGZJ FDA UDIIPF FDA UDI
- GMDN Term
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1500 FDA UDI882.5890 FDA UDI890.5850 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 4 Inch FDA UDI
Category: Physical therapy transcutaneous neuromuscular electrical stimulation system
e-vive NMES Electrode Set with Hook Backings by Motive Health, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Motive Health, Inc.
Sources (1)
- FDA UDI 00192af0-1155-4e78-b3de-520ff03c2616 37 fields · synced May 30, 2026