| Primary Device ID | 10810170012508 |
| NIH Device Record Key | 33759971-06fa-4239-855b-d915e9973636 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Azur Pushable Helical |
| Version Model Number | 45-250610 |
| Catalog Number | 45-250610 |
| 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 | 00810170012501 [Primary] |
| GS1 | 10810170012508 [Package] Contains: 00810170012501 Package: Carton [3 Units] In Commercial Distribution |
| 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 |
| 10810170017473 | Azur |
| 10810170017466 | Azur |
| 10810170017459 | Azur |
| 10810170017442 | Azur |
| 10810170017435 | Azur |
| 10810170017428 | Azur |
| 10810170017411 | Azur |
| 10810170017404 | Azur |
| 10810170014496 | Azur |
| 10810170012577 | Azur |
| 10810170012560 | Azur |
| 10810170012553 | Azur |
| 10810170012546 | Azur |
| 10810170012539 | Azur |
| 10810170012522 | Azur |
| 10810170012515 | Azur |
| 10810170012508 | Azur |
| 10810170012492 | Azur |
| 10810170012485 | Azur |
| 10810170012478 | Azur |
| 10810170012461 | Azur |
| 10810170012454 | Azur |
| 10810170012447 | Azur |
| 10810170012270 | Azur |
| 10810170012263 | Azur |
| 10810170012256 | Azur |
| 10810170012249 | Azur |
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| 10810170012157 | Azur |
| 10810170012140 | Azur |
| 10810170012133 | Azur |