ClearChart4 13795
Ref 13795
ClearChart4 13795 is a Class I device made by Reichert Inc., registered in EUDAMED on 23 Feb 2026 (Basic UDI-DI 081255901CLC001T3) and listed in FDA GUDID since 12 Aug 2025 (UDI-DI 00812559012201), active as of 25 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 | Number081255901CLC001T3 00812559012201 | Date23 Feb 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00812559012201 | Date12 Aug 2025 | StatusListed |
Official records
- EUDAMED public site 081255901CLC001T3
- AccessGUDID record 00812559012201
Across registries
- EUDAMED Basic UDI-DI 081255901CLC001T3 registered 23 Feb 2026 Active
- FDA GUDID UDI-DI 00812559012201 listed 12 Aug 2025 Listed
Timeline
- Listed FDA GUDID 00812559012201
- Registered EUDAMED 081255901CLC001T3
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- ClearChart 4 EUDAMEDClearChart4 GUDID
- Generic name
- Vision testing/training chart
- Device name
- ClearChart® 4
- Model / reference
- 13795
- Primary DI / UDI-DI
- 00812559012201
- Basic UDI-DI
- 081255901CLC001T3
- FDA product code
- HOX
- EMDN code
- Z1212012001 Visual functional assessment equipment
- GMDN term
- Vision testing/training chart
- Device class
- Class I
- Regulation number
- 886.1150
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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