| Primary Device ID | 00815165020202 |
| NIH Device Record Key | b4e8cc22-a6bc-4f69-b1ce-eabc5b091dab |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | I125 Calibration Seed |
| Version Model Number | I125 Calibration Seed |
| Catalog Number | I125SEEDCAL |
| Company DUNS | 021125001 |
| Company Name | Eckert & Ziegler Bebig, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |