| Primary Device ID | 05415067020499 |
| NIH Device Record Key | 601c39ee-60f1-4736-a7e0-dadce80244f4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MediGuide¿™ |
| Version Model Number | Technology |
| Catalog Number | MG1000 |
| Company DUNS | 149818952 |
| Company Name | ST. JUDE MEDICAL, INC. |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |