| Primary Device ID | 20850035767614 |
| NIH Device Record Key | 6f71bd3c-2cc8-44b0-8481-834df76a9c01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IOB |
| Version Model Number | IOB-011S |
| 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 | 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |