| Primary Device ID | 16944413824949 |
| NIH Device Record Key | 23a9d8aa-e49c-4c57-878e-b70a673419b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RespArray ECG whole cable |
| Version Model Number | 01.57.472334 |
| Company DUNS | 529173163 |
| Company Name | Edan Instruments, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06944413824942 [Primary] |
| GS1 | 16944413824949 [Package] Contains: 06944413824942 Package: [10 Units] In Commercial Distribution |
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-09 |
| Device Publish Date | 2022-09-01 |
| 06944413826199 | 01.57.472398 |
| 06944413826182 | 01.57.472397 |
| 06944413826175 | 01.57.472396 |
| 06944413826168 | 01.57.472395 |
| 16944413825090 | 01.57.472352 |
| 16944413825083 | 01.57.472351 |
| 16944413825076 | 01.57.472350 |
| 16944413825069 | 01.57.472349 |
| 16944413825038 | 01.57.472344 |
| 16944413825021 | 01.57.472343 |
| 16944413825014 | 01.57.472342 |
| 16944413825007 | 01.57.472341 |
| 16944413824970 | 01.57.472337 |
| 16944413824963 | 01.57.472336 |
| 16944413824956 | 01.57.472335 |
| 16944413824949 | 01.57.472334 |
| 16944413824895 | 01.57.472326 |
| 16944413824888 | 01.57.472325 |
| 16944413824871 | 01.57.472324 |
| 16944413824864 | 01.57.472323 |