| Primary Device ID | 08586014620073 |
| NIH Device Record Key | 141648ae-5004-4d21-b447-959e793b2b51 |
| Commercial Distribution Discontinuation | 2018-09-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | E1 |
| Version Model Number | 220-240V/50-60Hz |
| Company DUNS | 360551766 |
| Company Name | EKOM spol. s r.o. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 |