Vein Illuminator NAVI-60
by Medcaptain Medical Technology Co., Ltd.
Ref /Model NAVI-30, NAVI-60
Vein Illuminator NAVI-60 is a Class I device made by Medcaptain Medical Technology Co., Ltd., registered in EUDAMED on 28 May 2026 (Basic UDI-DI 69268026MV01000001VZ) and listed in FDA GUDID since 5 Feb 2024 (UDI-DI 06926802602812), active as of 22 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 | Number69268026MV01000001VZ 06926802602812 | Date28 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number06926802602812 | Date5 Feb 2024 | StatusListed |
Official records
- EUDAMED public site 69268026MV01000001VZ
- AccessGUDID record 06926802602812
Across registries
- EUDAMED Basic UDI-DI 69268026MV01000001VZ registered 28 May 2026 Active
- FDA GUDID UDI-DI 06926802602812 listed 5 Feb 2024 Listed
Timeline
- Listed FDA GUDID 06926802602812
- Registered EUDAMED 69268026MV01000001VZ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Vein Illuminator
- Generic name
- Infrared-light vein locator
- Model / reference
- NAVI-30, NAVI-60, /
- Primary DI / UDI-DI
- 06926802602812
- Basic UDI-DI
- 69268026MV01000001VZ
- FDA product code
- KZA
- EMDN code
- V9099 Various devices not included in other classes - other
- GMDN term
- Infrared-light vein locator
- Device class
- Class I
- Regulation number
- 880.6970
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | NAVI-30, NAVI-60 / | NAVI-60 |
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