| Primary Device ID | 00811425028711 |
| NIH Device Record Key | f7fbf7f3-4673-45d3-9aeb-8ab2192c0008 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cosmos 18 Advanced |
| Version Model Number | 8218-0617 |
| Catalog Number | 8218-0617 |
| Company DUNS | 003263105 |
| Company Name | MICROVENTION INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00811425028711 [Primary] |
| KRD | Device, Vascular, for Promoting Embolization |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-11-19 |
| Device Publish Date | 2015-12-29 |
| 00812636023410 | V-Trak |
| 00812636023403 | V-Trak |
| 00812636023397 | V-Trak |
| 00812636023380 | V-Trak |
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| 00812636023366 | V-Trak |
| 00812636023359 | V-Trak |
| 00812636023342 | V-Trak |
| 00812636023335 | V-Trak |
| 00812636023328 | V-Trak |
| 00812636023311 | V-Trak |
| 00812636023304 | V-Trak |
| 00812636023298 | V-Trak |
| 00812636023281 | V-Trak |
| 00812636023274 | V-Trak |
| 00811425028797 | V-Trak |
| 00811425028780 | V-Trak |
| 00811425028773 | V-Trak |
| 00811425028766 | V-Trak |
| 00811425028759 | V-Trak |
| 00811425028742 | V-Trak |
| 00811425028735 | V-Trak |
| 00811425028728 | V-Trak |
| 00811425028711 | V-Trak |