Ophthalmic Electric Table MD-V
by Mdt Sp Z O O
Part of a family of 20 devices: see the family page
Ref MD-V
Ophthalmic Electric Table MD-V is a Class I device made by Mdt Sp Z O O, registered in EUDAMED on 18 May 2026 (Basic UDI-DI 5907642694TABGF) and listed in FDA GUDID since 16 Jul 2025 (UDI-DI 05907642694275), 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 | Number5907642694TABGF 05907642694275 | Date18 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05907642694275 | Date16 Jul 2025 | StatusListed |
Official records
- EUDAMED public site 5907642694TABGF
- AccessGUDID record 05907642694275
Across registries
- EUDAMED Basic UDI-DI 5907642694TABGF registered 18 May 2026 Active
- FDA GUDID UDI-DI 05907642694275 listed 16 Jul 2025 Listed
Timeline
- Listed FDA GUDID 05907642694275
- Registered EUDAMED 5907642694TABGF
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Okulistyczny stolik elektryczny EUDAMEDOphthalmic Electric Table GUDID
- Generic name
- Ophthalmic instrument table, line-powered
- Device name
- Ophthalmic Electric Table / Okulistyczny stolik elektryczny
- Model / reference
- MD-V
- Primary DI / UDI-DI
- 05907642694275
- Basic UDI-DI
- 5907642694TABGF
- Direct marketing DI
- 05907642694275
- FDA product code
- HRJ
- EMDN code
- Q0299 Ophthalmic devices - other
- GMDN term
- Ophthalmic instrument table, line-powered
- Device class
- Class I
- Regulation number
- 886.4855
- EU registration type
- Standard device
- EU market of registration
- Poland
- GUDID distribution status
- In Commercial Distribution
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