| Primary Device ID | 10812444028826 |
| NIH Device Record Key | a5bcc4ea-5fdb-4710-b9b8-54ce7a4d160a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Gold Marker |
| Version Model Number | GM1032 |
| 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 | 00812444028829 [Primary] |
| GS1 | 10812444028826 [Package] Contains: 00812444028829 Package: [9 Units] In Commercial Distribution |
| GS1 | 20812444028823 [Package] Contains: 00812444028829 Package: [10 Units] In Commercial Distribution |
| GS1 | 30812444028820 [Package] Contains: 00812444028829 Package: [5 Units] In Commercial Distribution |
| NEU | Marker, Radiographic, Implantable |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-11-05 |
| Device Publish Date | 2018-10-03 |
| 10812444028826 | Gold Marker |
| 30812444027991 | GM1254 |
| 30812444027977 | Brachytherapy |
| 00812444027136 | BRACHYTHERAPY |
| 00812444025842 | BRACHYTHERAPY |
| 00812444024739 | BRACHYTHERAPY |
| 00812444024449 | BRACHYTHERAPY |
| 00812444023527 | BRACHYTHERAPY |
| 00812444023510 | BRACHYTHERAPY |
| 00812444023282 | BRACHYTHERAPY |
| 00812444023275 | BRACHYTHERAPY |
| 00812444022209 | Brachytherapy |
| 00812444022049 | SUTURE |
| 10810020083146 | Brachytherapy |
| 10810020083139 | Brachytherapy |