| Primary Device ID | 00810170017520 |
| NIH Device Record Key | 4f73cb23-12b1-482f-818d-19f9df498d36 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Azur CX Detachable |
| Version Model Number | 45-780828 |
| Catalog Number | 45-780828 |
| 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 | 00810170017520 [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 |
| 00810170018404 | Azur |
| 00810170018398 | Azur |
| 00810170018381 | Azur |
| 00810170018374 | Azur |
| 00810170018367 | Azur |
| 00810170018350 | Azur |
| 00810170018343 | Azur |
| 00810170018336 | Azur |
| 00810170018329 | Azur |
| 00810170018312 | Azur |
| 00810170018305 | Azur |
| 00810170018299 | Azur |
| 00810170017599 | Azur |
| 00810170017582 | Azur |
| 00810170017575 | Azur |
| 00810170017568 | Azur |
| 00810170017551 | Azur |
| 00810170017544 | Azur |
| 00810170017537 | Azur |
| 00810170017520 | Azur |
| 00810170017513 | Azur |
| 00810170017506 | Azur |
| 00810170017490 | Azur |
| 00810170017483 | Azur |
| 00812636021102 | Azur |
| 00812636021096 | Azur |
| 00812636021089 | Azur |
| 00812636021072 | Azur |
| 00812636021065 | Azur |
| 00812636021058 | Azur |
| 00812636021041 | Azur |
| 00812636021034 | Azur |
| 00812636021027 | Azur |
| 00812636021010 | Azur |