Identity
- Trade Name
- mo-vis FDA UDI
- Generic Name
- Wheelchair steering/control unit FDA UDI
- Device Name
- Sip and Puff Set Head Control FDA UDI
- Model / Reference
- P032-51 FDA UDI
- Description
- Sip and Puff Set Head Control FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05407008321116 FDA UDI
- FDA Product Code
- KNN FDA UDI
- GMDN Term
- Wheelchair steering/control unit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3920 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
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Wheelchair steering/control unit
mo-vis by mo-Vis — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wheelchair steering/control unit.
- Switch-It — Sunrise Medical (US) LLC · Class I
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- Switch-It Head Controls-External — Sunrise Medical (US) LLC · Class I
- CTRL+5, Dual Pro, Joystick in a Can, MicroGuide, MicroPilot, and Tough JoyStick — Sunrise Medical (US) LLC · Class I
- Remote Stop Switch — Sunrise Medical (US) LLC · Class I
- munevo DRIVE — Munevo Inc. · Class I
- Cool Cube / TouchDrive 2 — Sunrise Medical (US) LLC · Class I
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
- mo-Vis
Sources (1)
- FDA UDI 5b0a3562-1f5f-409f-995d-1d22b2990958 33 fields · synced May 30, 2026