Identity
- Trade Name
- NAVIONE FDA UDI
- Generic Name
- Wheelchair electric-motor-driven propulsion system FDA UDI
- Model / Reference
- X0EJ FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04580027190213 FDA UDI
- 510(k) Number
- K140204 FDA UDI
- FDA Product Code
- ITI FDA UDI
- GMDN Term
- Wheelchair electric-motor-driven propulsion system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.3860 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Wheelchair electric-motor-driven propulsion system
Navione by Yamaha Motor Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K140204 also covers:
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
- Yamaha Motor Co., Ltd.
Sources (1)
- FDA UDI d10e56ab-c0f1-46d0-bea5-2f8772bb6618 34 fields · synced Jun 8, 2026