| Primary Device ID | 00861578000355 |
| NIH Device Record Key | d409a307-0af3-490c-a9b9-020e499d1bf7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trice Tablet 2 |
| Version Model Number | T200-001R |
| Company DUNS | 009452895 |
| Company Name | TRICE MEDICAL, 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 | 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00861578000355 [Primary] |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-06-29 |
| 00861578000355 | Tablet for use with mi-eye 2 probe. Reburbished. |
| 00861578000348 | Tablet for use with mi-eye 2 probe |