| Primary Device ID | 00810170016196 |
| NIH Device Record Key | aa819223-65cc-4139-884f-5bddfdc1d486 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MicroPlex VFC |
| Version Model Number | VFC030606-V |
| Catalog Number | VFC030606-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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00810170016196 [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 | 2019-09-12 |
| Device Publish Date | 2019-09-04 |
| 00812636026237 | V-Trak |
| 00812636026220 | V-Trak |
| 00812636026190 | V-Trak |
| 00812636023519 | V-Trak |
| 00811425026212 | V-Trak |
| 00811425026205 | V-Trak |
| 00816777026279 | V-Trak |
| 00816777026262 | V-Trak |
| 00810170016271 | V-Trak |
| 00810170016264 | V-Trak |
| 00810170016257 | V-Trak |
| 00810170016233 | V-Trak |
| 00810170016226 | V-Trak |
| 00810170016219 | V-Trak |
| 00810170016202 | V-Trak |
| 00810170016196 | V-Trak |