| Primary Device ID | 00841034112327 |
| NIH Device Record Key | 0abfebc1-567c-4ac0-9a44-0c326221b7ec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PATIENT CABLE - 3 LEAD DU |
| Version Model Number | KCC009 |
| Catalog Number | KCC009 |
| Company DUNS | 066232067 |
| Company Name | RPI |
| 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 | true |
| 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 |