| Primary Device ID | 10857808005013 |
| NIH Device Record Key | c5e1fdba-0e88-4ee3-8a8c-7e8920a69fe1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AspireAssist A-Tube Pack |
| Version Model Number | 200-0044 |
| Catalog Number | 200-0044 |
| Company DUNS | 026281163 |
| Company Name | ASPIRE BARIATRICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | 877-312-0007 |
| quality@aspirebariatrics.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10857808005013 [Primary] |
| OYF | Aspiration Therapy System |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2016-07-25 |
| 10857808005419 - Aspire Introducer Needle | 2024-03-20 Introducer Needle |
| 10857808005891 - Aspire Venting Tube Kit | 2020-04-20 Aspire Venting Tube Kit |
| 10857808005013 - AspireAssist A-Tube Pack | 2019-10-07A-Tube Pack |
| 10857808005013 - AspireAssist A-Tube Pack | 2019-10-07 A-Tube Pack |
| 10857808005020 - AspireAssist A-Tube Kit | 2019-10-07 AspireAssist A-Tube Kit |
| 10857808005037 - AspireAssist A-Tube Kit | 2019-10-07 AspireAssist A-Tube Kit |
| 10857808005044 - AspireAssist A-Tube Kit | 2019-10-07 AspireAssist A-Tube Kit |
| 10857808005471 - AspireAssist A-Tube Kit | 2019-10-07 AspireAssist A-Tube Kit |