| Primary Device ID | 00850017626331 |
| NIH Device Record Key | a8517b0b-2b65-4d86-ac68-64ba3bbd9d53 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MSI |
| Version Model Number | MAX9000DK |
| Company DUNS | 118447158 |
| Company Name | Modern Surgical Instruments LLC |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |