| Primary Device ID | 30866479000115 |
| NIH Device Record Key | 0d83323d-a9c4-4373-957f-f9317f828f1a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BEACON |
| Version Model Number | BM1412-50-F-1 |
| Company DUNS | 078473721 |
| Company Name | SCION MEDICAL TECHOLOGIES, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00866479000114 [Primary] |
| GS1 | 30866479000115 [Package] Contains: 00866479000114 Package: [10 Units] In Commercial Distribution |
| NEU | Marker, Radiographic, Implantable |
| 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 | 2016-09-30 |
| 30866479000115 | Beacon Tissue Marker/Beacon Tissue Marker (SE) is a sterile, single patient use, PEKK discrete m |
| 00866479000107 | Beacon Tissue Marker/Beacon Tissue Marker (SE) is a sterile, single patient use, PEKK discrete m |