| Primary Device ID | M68984493090 |
| NIH Device Record Key | e1db36e4-327e-4ff3-bff2-a28bb77997b6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mojo Direct Action Bag - Intermediate |
| Version Model Number | 09 |
| Catalog Number | 84-493 |
| Company DUNS | 118492643 |
| Company Name | Safeguard US Operating, LLC |
| 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 | 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 |
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