| Primary Device ID | 00860009184503 |
| NIH Device Record Key | bd9ab582-3372-4f8e-a772-7ff0ee63468f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BeamSite |
| Version Model Number | BeamSite |
| Company DUNS | 079605332 |
| Company Name | Doseoptics 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860009184503 [Primary] |
| IYE | Accelerator, Linear, Medical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-18 |
| Device Publish Date | 2023-08-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BEAMSITE 97163877 not registered Live/Pending |
DoseOptics LLC 2021-12-09 |