| Primary Device ID | 09348227000160 |
| NIH Device Record Key | 70d0d2a3-ab4d-4e81-aee9-32af7ad8895a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VorOtek M Scope |
| Version Model Number | VSMS |
| Catalog Number | VSMS |
| Company DUNS | 744332997 |
| Company Name | VOROTEK PTY LTD |
| 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 | 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 |