| Primary Device ID | 00841034112334 |
| NIH Device Record Key | 3efde6bb-1cbb-4441-b0e0-6c9569140aae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PATIENT CABLE - 3 LEAD DU |
| Version Model Number | KCC012 |
| Catalog Number | KCC012 |
| 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 |