| Primary Device ID | 00861001002628 |
| NIH Device Record Key | 88fe09e0-932b-4a71-80a7-70cad5a2afc6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Domico Med-Device, LLC |
| Version Model Number | 425 |
| Company DUNS | 081253414 |
| Company Name | DOMICO MED-DEVICE, LLC |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |