Illuminated Phoropter 11637
Ref 11637Model 11636
Illuminated Phoropter 11637 is a Class I device made by Reichert Inc., registered in EUDAMED on 11 Mar 2026 (Basic UDI-DI 081255901MNP0012R) and listed in FDA GUDID since 12 Aug 2025 (UDI-DI 00812559010320), 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 | Number081255901MNP0012R 00812559010320 | Date11 Mar 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00812559010320 | Date12 Aug 2025 | StatusListed |
Official records
- EUDAMED public site 081255901MNP0012R
- AccessGUDID record 00812559010320
Across registries
- EUDAMED Basic UDI-DI 081255901MNP0012R registered 11 Mar 2026 Active
- FDA GUDID UDI-DI 00812559010320 listed 12 Aug 2025 Listed
Timeline
- Listed FDA GUDID 00812559010320
- Registered EUDAMED 081255901MNP0012R
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Illuminated Phoroptor® EUDAMEDIlluminated Phoropter GUDID
- Generic name
- Phoropter, manual
- Model / reference
- 11637, 11636
- Primary DI / UDI-DI
- 00812559010320
- Basic UDI-DI
- 081255901MNP0012R
- FDA product code
- HKN
- EMDN code
- Z12120115 Optometers
- GMDN term
- Phoropter, manual
- Device class
- Class I
- Regulation number
- 886.1770
- System or procedure pack
- Procedure pack which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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