| Primary Device ID | 00810170017711 |
| NIH Device Record Key | e2ca75f4-69d6-4db7-b47c-d0bbe7b750de |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Azur Detachable Framing Coil |
| Version Model Number | 45-680512 |
| Catalog Number | 45-680512 |
| 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 | 00810170017711 [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 | 2015-12-29 |
| 00810170017834 | Azur |
| 00810170017827 | Azur |
| 00810170017810 | Azur |
| 00810170017803 | Azur |
| 00810170017797 | Azur |
| 00810170017780 | Azur |
| 00810170017773 | Azur |
| 00810170017766 | Azur |
| 00810170017759 | Azur |
| 00810170017742 | Azur |
| 00810170017735 | Azur |
| 00810170017728 | Azur |
| 00810170017711 | Azur |
| 00810170017704 | Azur |
| 00810170016158 | Azur |
| 00810170016141 | Azur |
| 00810170016134 | Azur |
| 00810170016127 | Azur |
| 00810170016110 | Azur |
| 00810170016103 | Azur |
| 00810170016097 | Azur |
| 00810170013737 | Azur |
| 00810170013720 | Azur |
| 00810170013713 | Azur |
| 00810170013706 | Azur |
| 00810170013690 | Azur |
| 00810170013683 | Azur |
| 00810170013676 | Azur |
| 00810170013669 | Azur |
| 00810170013652 | Azur |
| 00810170013645 | Azur |
| 00810170013638 | Azur |
| 00810170013621 | Azur |
| 00810170013614 | Azur |
| 00810170013607 | Azur |