| Primary Device ID | 00850007069711 |
| NIH Device Record Key | f3b1d956-5701-4ff3-a3ae-2322497b92df |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MISScope 4K |
| Version Model Number | VSY-2260 |
| Company DUNS | 096680671 |
| Company Name | VISEON, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 00850007069711 [Primary] |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-13 |
| Device Publish Date | 2024-02-05 |
| 00850007069735 | MISScope 4K, 22 Dia, 80L |
| 00850007069728 | MISScope 4K, 22 Dia, 70L |
| 00850007069711 | MISScope 4K, 22 Dia, 60L |
| 00850007069704 | MISScope 4K, 22 Dia, 50L |
| 00850007069698 | MISScope 4K, 22 Dia, 40L |
| 00850007069681 | MISScope 4K, 18 Dia, 80L |
| 00850007069674 | MISScope 4K, 18 Dia, 70L |
| 00850007069667 | MISScope 4K, 18 Dia, 60L |
| 00850007069643 | MISScope 4K, 18 Dia, 40L |
| 00850007069650 | MISScope 4K, 18 Dia, 50L |