| Primary Device ID | 00810170014185 |
| NIH Device Record Key | 31badb9d-4130-4136-849c-87f2d2974e07 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MicroPlex Cosmos |
| Version Model Number | 182065CS-V |
| Catalog Number | 182065CS-V |
| 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 | 00810170014185 [Primary] |
| HCG | DEVICE, NEUROVASCULAR EMBOLIZATION |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-07 |
| Device Publish Date | 2018-08-07 |
| 00811425023488 | V-Trak |
| 00810170014338 | V-Trak |
| 00810170014222 | V-Trak |
| 00810170014215 | V-Trak |
| 00810170014208 | V-Trak |
| 00810170014192 | V-Trak |
| 00810170014185 | V-Trak |
| 00810170014178 | V-Trak |
| 00810170014161 | V-Trak |
| 00810170014147 | V-Trak |
| 00810170014130 | V-Trak |
| 00810170014123 | V-Trak |
| 00810170014116 | V-Trak |
| 00810170014109 | V-Trak |
| 00810170014093 | V-Trak |
| 00810170014086 | V-Trak |
| 00810170014079 | V-Trak |
| 00810170014062 | V-Trak |
| 00810170014055 | V-Trak |
| 00810170014048 | V-Trak |
| 00810170013591 | V-Trak |
| 00810170013584 | V-Trak |
| 00810170013577 | V-Trak |
| 00810170013553 | V-Trak |
| 00810170013546 | V-Trak |
| 00810170013539 | V-Trak |
| 00810170013522 | V-Trak |
| 00810170013515 | V-Trak |
| 00810170013508 | V-Trak |
| 00810170013492 | V-Trak |
| 00816777024152 | V-Trak |
| 04987350314031 | V-Trak |
| 00810170014154 | V-Trak |
| 00810170014031 | V-Trak |
| 00810170013560 | V-Trak |