| Primary Device ID | B3902272041 |
| NIH Device Record Key | b6c72b14-ef40-43e4-97b1-1f62a692834a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reprocessed Premier 90 Electrode, 3.3mm |
| Version Model Number | 227204 |
| Company DUNS | 785616934 |
| Company Name | SURETEK MEDICAL |
| 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 | true |
| OTC Over-The-Counter | false |