| Primary Device ID | 00850035767009 |
| NIH Device Record Key | 9e692401-2054-4daa-8f45-fb4567ca8e1b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IOB |
| Version Model Number | IOB-505 |
| Company DUNS | 040239376 |
| Company Name | Iob Medical Inc. |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |