| Primary Device ID | 00815871020763 |
| NIH Device Record Key | 72982224-440a-4e38-9e9e-33d838c036b0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | True ECG 12 |
| Version Model Number | 60136 |
| Company DUNS | 178440426 |
| Company Name | Avante |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com | |
| Phone | 502-244-4444 |
| devicehelp@dremed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00815871020763 [Primary] |
| DPS | Electrocardiograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-06-19 |
| Device Publish Date | 2016-09-23 |
| 00815871020817 | 60126SS |
| 00815871020800 | 60126ISS |
| 00815871020794 | 60126I |
| 00815871020787 | 60126 |
| 00815871020770 | 60136S |
| 00815871020763 | 60136 |