| Primary Device ID | 07290107981712 |
| NIH Device Record Key | 6e0f0089-c12d-41c3-a520-c94a36ca32be |
| Commercial Distribution Discontinuation | 2019-04-23 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Device Bag for the Optune |
| Version Model Number | BAG 9000_GRAY |
| Catalog Number | 90002 |
| Company DUNS | 056552035 |
| Company Name | NOVOCURE 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 | true |
| Serial Number | false |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep indoors |
| Special Storage Condition, Specify | Between 0 and 0 *Keep indoors |
| Special Storage Condition, Specify | Between 0 and 0 *Keep indoors |
| Special Storage Condition, Specify | Between 0 and 0 *Keep indoors |
| Special Storage Condition, Specify | Between 0 and 0 *Keep indoors |
| Special Storage Condition, Specify | Between 0 and 0 *Keep indoors |
| Special Storage Condition, Specify | Between 0 and 0 *Keep indoors |