| Primary Device ID | 90815187020177 |
| NIH Device Record Key | 0679fffc-39f9-4221-88f9-86371636edd2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Patient Cable |
| Version Model Number | 001-400-0002 |
| Catalog Number | 001-400-0002 |
| Company DUNS | 147035427 |
| Company Name | GLOBAL INSTRUMENTATION, LLC |
| 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 | true |
| OTC Over-The-Counter | false |
| 90815187020351 | 5 Lead Patient Cable, IEC, M3R |
| 90815187020238 | 7 Lead Patient Cable, IEC, HR100 |
| 90815187020221 | 7 Lead Patient Cable, AHA, HR100 |
| 90815187020214 | 5-Lead Patient Cable, IEC |
| 90815187020207 | 5-Lead Patient Cable, AHA, HR100 |
| 90815187020191 | M12R, 10 Lead Patient Cable |
| 90815187020184 | M12R, 10 Lead patient Cable (DIN) |
| 90815187020177 | M12R, 10 Lead patient Cable (AHA) |
| 90815187020160 | M3R/M12R, 7 Lead patient Cable |
| 90815187020153 | M3R/M12R, 7 Lead patient Cable (AHA) |
| 90815187020146 | 7 Lead Patient Cable, IEC, HR300 |
| 90815187020139 | 7 Lead Patient Cable, AHA, HR300 |
| 90815187020122 | 5 Lead Patient Cable, IEC, HR300 |
| 90815187020078 | Patient Cable 3L IEC |
| 90815187020061 | Patient Cable 5L IEC |
| 90815187020054 | Patient Cable 3L AHA |
| 90815187020009 | Patient Cable 5L AHA |