| Primary Device ID | 10817417021811 |
| NIH Device Record Key | 73848fd4-b22a-4764-afda-22c99766789a |
| Commercial Distribution Discontinuation | 2032-11-01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aseptico Technique |
| Version Model Number | AMA-09A2 |
| Company DUNS | 016853348 |
| Company Name | ASEPTICO, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |