| Primary Device ID | 00860002090191 |
| NIH Device Record Key | a1622915-9ef3-4edd-a3cb-0cc3fe64706a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Rampart |
| Version Model Number | L148-TMS |
| Company DUNS | 117119538 |
| Company Name | Rampart Ic, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00860002090191 [Primary] |
| EAK | Screen, Leaded, Operator Radiation Protector |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-04 |
| Device Publish Date | 2023-08-25 |
| 00860002090191 | Table Mounting Shield |
| 00860002090184 | Radiation Shield |
| 00860002090177 | Radiation Shield |
| 00860002090108 | Radiation Shielding Panel, portal/mobile |