| Primary Device ID | 10815411020588 |
| NIH Device Record Key | 5b4ffe84-8c99-448e-9713-71b413864982 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OPTION, EXTENDED SCANBOARD SHORT POST WITH TARGET |
| Version Model Number | 0-00202-002 |
| Company DUNS | 145008178 |
| Company Name | NEUROLOGICA CORP. |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10815411020588 [Primary] |
| JAK | System, X-Ray, Tomography, Computed |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-12-14 |
| Device Publish Date | 2021-12-06 |
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