| Primary Device ID | 10810020082064 |
| NIH Device Record Key | 96accc87-89e3-44cd-aeab-c5023b499118 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Riverpoint Brachytherapy |
| Version Model Number | 1100-1820X-5-F |
| 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 | 00810020082067 [Primary] |
| GS1 | 10810020082064 [Package] Contains: 00810020082067 Package: [10 Units] In Commercial Distribution |
| GS1 | 20810020082061 [Package] Contains: 00810020082067 Package: [9 Units] In Commercial Distribution |
| KXK | Source, Brachytherapy, Radionuclide |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-10-10 |
| Device Publish Date | 2019-10-02 |