Neuronavigator QuickVision
by Shenzhen Yingzhi Technology Co., Ltd.
Neuronavigator QuickVision is a Class II device made by Shenzhen Yingzhi Technology Co., Ltd., listed in FDA GUDID since 21 Aug 2026 (UDI-DI 06971538581788), registry data as of 22 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 | Number06971538581788 | Date21 Aug 2026 | StatusListed |
Official records
- AccessGUDID record 06971538581788
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Neuronavigator
- Generic name
- Magnetic neural stimulation system
- Model / reference
- QuickVision
- Primary DI / UDI-DI
- 06971538581788
- FDA product code
- OBP
- GMDN term
- Magnetic neural stimulation system
- Device class
- Class II
- Regulation number
- 882.5805
- GUDID distribution status
- In Commercial Distribution
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