MotionVR
by Virtualis
MotionVR is a Class I device made by Virtualis, listed in FDA GUDID since 8 Oct 2021 (UDI-DI 03760310780562), registry data as of 31 May 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03760310780562 | Date8 Oct 2021 | StatusListed |
Official records
- AccessGUDID record 03760310780562
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Posturography system platform
- Model / reference
- MOT
- Primary DI / UDI-DI
- 03760310780562
- FDA product code
- KHX
- GMDN term
- Posturography system platform
- Device class
- Class I
- Regulation number
- 890.1575
- GUDID distribution status
- In Commercial Distribution
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