| Primary Device ID | 00854362008545 |
| NIH Device Record Key | baca4b57-ab8e-410f-857f-2a0d59a10f2b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Assembly Required Distributors Inc. |
| Version Model Number | 0000-233 |
| Company DUNS | 170562396 |
| Company Name | Assembly Required Distributors Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| 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 | false |
| OTC Over-The-Counter | false |