Visionix VX40
by Luneau Technology Operations
Ref VX40
Visionix VX40 is a Class I device made by Luneau Technology Operations, registered in EUDAMED on 7 May 2026 (Basic UDI-DI 13664188000329M3) and listed in FDA GUDID since 8 Jun 2023 (UDI-DI 03664188000329), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number13664188000329M3 03664188000329 | Date7 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03664188000329 | Date8 Jun 2023 | StatusListed |
Official records
- EUDAMED public site 13664188000329M3
- AccessGUDID record 03664188000329
Across registries
- EUDAMED Basic UDI-DI 13664188000329M3 registered 7 May 2026 Active
- FDA GUDID UDI-DI 03664188000329 listed 8 Jun 2023 Listed
Timeline
- Listed FDA GUDID 03664188000329
- Registered EUDAMED 13664188000329M3
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- VX40 EUDAMEDVisionix GUDID
- Generic name
- Automated lensmeter
- Model / reference
- VX40
- Primary DI / UDI-DI
- 03664188000329
- Basic UDI-DI
- 13664188000329M3
- Direct marketing DI
- 03664188000329
- FDA product code
- HLM
- EMDN code
- Q0299 Ophthalmic devices - other
- GMDN term
- Automated lensmeter
- Device class
- Class I
- Regulation number
- 886.1425
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
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