| Primary Device ID | 00812444022100 |
| NIH Device Record Key | 9cd3e041-e976-46e9-a035-cff4ae00c01f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RIVERPOINT BRACHYTHERAPY |
| Version Model Number | GM1051-1820 |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | 00812444022100 [Primary] |
| GS1 | 20812444022104 [Package] Package: [10 Units] In Commercial Distribution |
| GS1 | 30812444022101 [Package] Package: [9 Units] In Commercial Distribution |
| GS1 | 40812444022108 [Package] Package: [5 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 | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-22 |