| Primary Device ID | 50604351601258 |
| NIH Device Record Key | f4f711f0-08c3-43c3-a8f0-4ba57ef81882 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AeroEclips*BAN* |
| Version Model Number | AE II BAN & Filtered Mouthpiece, cs/25 |
| Company DUNS | 056332380 |
| Company Name | Monaghan Medical 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
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| 50604351501121 - Aerochamber Plus® Flow-Vu® | 2023-11-22 AC Plus, Flow-Vu aVHC, Small Mask, Retail - 50112 |
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| 50604351503125 - Aerochamber Plus® Flow-Vu® | 2023-11-22 AC Plus, Flow-Vu aVHC, Large Mask, Retail - 50312 |
| 50604351601258 - AeroEclips*BAN* | 2023-09-14AE II BAN with Universal Tubing & Filtered Mouthpiece Kit, cs/25 |
| 50604351601258 - AeroEclips*BAN* | 2023-09-14 AE II BAN with Universal Tubing & Filtered Mouthpiece Kit, cs/25 |