| Primary Device ID | 00860624000431 |
| NIH Device Record Key | bf9765ac-8ab1-4c1b-a63b-eb32c5f86a6a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AURORA Evacuator |
| Version Model Number | AURORA Evacuator-7 |
| Catalog Number | AURORA Evacuator-7 |
| Company DUNS | 080909607 |
| Company Name | REBOUND THERAPEUTICS CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860624000431 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-06-29 |
| Device Publish Date | 2018-05-29 |
| 00860624000431 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00860624000424 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00860624000417 | The AURORA Evacuator is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332087 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332070 | The AURORA Evacuator is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332063 | The AURORA Evacuator is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332025 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332018 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332001 | The AURORA Evacuator is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332162 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332155 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |
| 00850002332148 | The Aurora EVACUATOR is provided sterile, for single-use only. It is a disposable, handheld, asp |