| Primary Device ID | 00812444023206 |
| NIH Device Record Key | 2ff5c4ce-7317-454d-8bad-ac50191613c7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RIVERPOINT BRACHYTHERAPY |
| Version Model Number | GM1231-1730 |
| 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 | 00812444023206 [Primary] |
| GS1 | 10812444023203 [Package] Package: [5 Units] In Commercial Distribution |
| GS1 | 20812444023200 [Package] Package: [9 Units] In Commercial Distribution |
| GS1 | 30812444023207 [Package] Package: [10 Units] In Commercial Distribution |
| KXK | Source, Brachytherapy, Radionuclide |
| 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 | 2015-10-22 |