| Primary Device ID | 00816777025456 |
| NIH Device Record Key | 307650a1-d541-4451-bcbb-96615c5f8ab9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HydroSoft 3D |
| Version Model Number | 7110-0304-3D-A2 |
| Catalog Number | 7110-0304 |
| 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 Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816777025456 [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 | 2 |
| Public Version Date | 2018-11-23 |
| Device Publish Date | 2018-08-07 |
| 00810170016554 | V-Trak |
| 00812636026596 | V-Trak |
| 00812636025483 | V-Trak |
| 00812636025414 | V-Trak |
| 00811425026564 | V-Trak |
| 00811425026489 | V-Trak |
| 00816777026583 | V-Trak |
| 00816777026576 | V-Trak |
| 00816777026545 | V-Trak |
| 00816777026538 | V-Trak |
| 00816777026521 | V-Trak |
| 00816777026514 | V-Trak |
| 00816777026507 | V-Trak |
| 00816777026491 | V-Trak |
| 00816777026477 | V-Trak |
| 00816777026453 | V-Trak |
| 00816777026446 | V-Trak |
| 00816777026439 | V-Trak |
| 00816777025470 | V-Trak |
| 00816777025456 | V-Trak |
| 00816777025449 | V-Trak |
| 00816777025432 | V-Trak |
| 00816777025401 | V-Trak |
| 00816777025395 | V-Trak |
| 00816777025388 | V-Trak |
| 00816777025371 | V-Trak |
| 00816777025357 | V-Trak |
| 00816777025340 | V-Trak |
| 00816777025333 | V-Trak |
| 00816777025326 | V-Trak |
| 00816777025319 | V-Trak |
| 00816777026590 | V-Trak |
| 00816777026569 | V-Trak |
| 00816777026484 | V-Trak |
| 00816777025487 | V-Trak |
| 00816777025418 | V-Trak |