CrowdVR v1.3.2
by Virtualis
CrowdVR v1.3.2 is a Class II device made by Virtualis, listed in FDA GUDID since 8 Oct 2021 (UDI-DI 03760310780241), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03760310780241 | Date8 Oct 2021 | StatusListed |
Official records
- AccessGUDID record 03760310780241
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- CrowdVR
- Generic name
- Biomechanical function analysis/rehabilitation software
- Model / reference
- v1.3.2
- Primary DI / UDI-DI
- 03760310780241
- FDA product code
- ISD
- GMDN term
- Biomechanical function analysis/rehabilitation software
- Device class
- Class II
- Regulation number
- 890.5360
- GUDID distribution status
- In Commercial Distribution
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