| Primary Device ID | 00812444023497 |
| NIH Device Record Key | eb5b9e34-ee06-4a8d-af95-b3470af4748b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RIVERPOINT BRACHYTHERAPY |
| Version Model Number | GM0453-2020 |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, 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 | 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812444023497 [Primary] |
| GS1 | 10812444023494 [Package] Package: [5 Units] In Commercial Distribution |
| GS1 | 20812444023491 [Package] Package: [9 Units] In Commercial Distribution |
| GS1 | 30812444023498 [Package] Package: [10 Units] In Commercial Distribution |
| IYE | Accelerator, Linear, Medical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2018-07-12 |
| Device Publish Date | 2015-10-24 |