| Primary Device ID | 00811425028520 |
| NIH Device Record Key | 92ce3ad2-c4a5-446c-a35c-5ac5586cfaab |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Helical Regular 18 Advanced |
| Version Model Number | 8618-1230 |
| Catalog Number | 8618-1230 |
| 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 | 00811425028520 [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 | 2016-09-24 |
| 00812636023120 | V-Trak |
| 00812636023113 | V-Trak |
| 00812636023106 | V-Trak |
| 00812636023090 | V-Trak |
| 00812636023083 | V-Trak |
| 00812636023076 | V-Trak |
| 00812636023069 | V-Trak |
| 00812636023052 | V-Trak |
| 00812636023045 | V-Trak |
| 00812636023038 | V-Trak |
| 00812636023014 | V-Trak |
| 00811425028568 | V-Trak |
| 00811425028551 | V-Trak |
| 00811425028544 | V-Trak |
| 00811425028537 | V-Trak |
| 00811425028520 | V-Trak |
| 00811425028513 | V-Trak |
| 00811425028506 | V-Trak |
| 00811425028490 | V-Trak |
| 00811425028483 | V-Trak |
| 00811425028476 | V-Trak |
| 00811425028469 | V-Trak |