| Primary Device ID | 04987350310279 |
| NIH Device Record Key | 30b44ef4-fa42-4694-af2e-9afa6cadc66e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MicroPlex HyperSoft Helical |
| Version Model Number | 100202HS-V |
| Catalog Number | 100202HS-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 |
| Phone | +1(714)247-8000 |
| customerservice@microvention.c |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04987350310279 [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 |
| 00811425020296 | V-Trak |
| 00810170010408 | V-Trak |
| 00810170010392 | V-Trak |
| 00810170010385 | V-Trak |
| 00810170010378 | V-Trak |
| 00810170010361 | V-Trak |
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| 00810170010347 | V-Trak |
| 00810170010330 | V-Trak |
| 00810170010323 | V-Trak |
| 00810170010316 | V-Trak |
| 00810170010309 | V-Trak |
| 00810170010286 | V-Trak |
| 00810170010262 | V-Trak |
| 04987350310279 | V-Trak |
| 00810170010279 | V-Trak |