| Primary Device ID | 05907642694312 |
| NIH Device Record Key | 7cd84580-a9f3-44f6-a3a3-553a0d4fc7e2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ophthalmic Electric Table |
| Version Model Number | MD-3V |
| Company DUNS | 366126408 |
| Company Name | MDT SP Z O O |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05907642694312 [Primary] |
| HRJ | Table, Instrument, Powered, Ophthalmic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-24 |
| Device Publish Date | 2025-07-16 |
| 05907642694107 | MD-1 |
| 05907642694244 | MD-X |
| 05907642694350 | TT2C-1000 |
| 05907642694343 | TT2C-800 |
| 05907642694336 | RT 2C |
| 05907642694329 | MD-3 |
| 05907642694312 | MD-3V |
| 05907642694305 | TTVS-1000 |
| 05907642694299 | RT V |
| 05907642694282 | TT-1060 |
| 05907642694275 | MD-V |
| 05907642694268 | RT B |
| 05907642694237 | COMBO-2 |
| 05907642694220 | RT VF |
| 05907642694213 | TTH-1000 |
| 05907642694206 | MD-2 |
| 05907642694190 | TT-4060 |
| 05907642694183 | RT S |
| 05907642694176 | COMBO-1 |
| 05907642694169 | TTUD-1000 |