| Primary Device ID | 00850359007805 |
| NIH Device Record Key | cafe3334-2806-4af4-bcaf-a5367017032e |
| Commercial Distribution Discontinuation | 2030-02-28 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Larson Bladed Lancet |
| Version Model Number | NGS-BL-01 |
| Catalog Number | NGS-BL-01 |
| Company DUNS | 959181160 |
| Company Name | CLEARPOINT NEURO, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850359007805 [Primary] |
| HAO | Instrument, Surgical, Non-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-02-01 |
| Device Publish Date | 2021-01-22 |
| 08503590070801 | Bladed Lancet |
| 00850359007805 | Bladed Lancet |