| Primary Device ID | 00857398006325 |
| NIH Device Record Key | 545145b8-673d-4753-8ba9-c756e827c8c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GS-26 |
| Version Model Number | Disposable ECG-EMG electrode |
| Company DUNS | 154714232 |
| Company Name | MULTI BIOSENSORS, INC. |
| Device Count | 150 |
| 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 | 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 |
| Phone | 915-581-9684 |
| harold@multibiosensors.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00857398006318 [Unit of Use] |
| GS1 | 00857398006325 [Primary] |
| DRX | Electrode, Electrocardiograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-10-26 |
| 00857398006509 - FEP001 | 2019-10-25 |
| 00857398006158 - 2DT2 | 2018-06-18 |
| 00857398006363 - NET3 | 2018-05-17 |
| 20857398006244 - DE-301 | 2018-03-29 |
| 00857398006455 - 4630 | 2018-03-29 |
| 00857398006479 - GS27 | 2018-03-29 |
| 00857398006264 - 3ST3-P | 2018-03-29 |
| 00857398006387 - 3PT3-6 | 2018-03-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GS-26 73208007 1174408 Dead/Cancelled |
Diamond Shamrock Corporation 1979-03-19 |