| Primary Device ID | B227NRP1302 |
| NIH Device Record Key | 4ca72ab2-1ab0-44e5-b86f-317ec66c8e45 |
| Commercial Distribution Discontinuation | 2030-11-24 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter |
| Version Model Number | R-417-156 |
| Catalog Number | R-417-156 |
| Company DUNS | 608625823 |
| Company Name | NORTH EAST SCIENTIFIC INC |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |