| Primary Device ID | 17290013745610 |
| NIH Device Record Key | 951a11f3-486a-4c6a-8a97-2230b2a0913f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VivaSight-DL |
| Version Model Number | DLVT39 |
| Catalog Number | DLVT39 |
| Company DUNS | 534096359 |
| Company Name | E.T. VIEW LTD |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| 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 |
| Phone | +972-722607060 |
| medical@ETView.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290013745613 [Primary] |
| GS1 | 17290013745610 [Package] Contains: 07290013745613 Package: carton [5 Units] In Commercial Distribution |
| GS1 | 27290013745617 [Package] Package: Carton [2 Units] In Commercial Distribution |
| CBI | Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[17290013745610]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-08-15 |
| Device Publish Date | 2016-09-24 |
| 27290013745624 | Visualized double lumen endobronchial tube set. The set contains DL tube, two pouches of suctio |
| 17290013745610 | Visualized double lumen endobronchial tube set. The set contains 1 DL tube, two pouches of sucti |
| 07290013745606 | Visualized double lumen endobronchial tube set. The set contains 1 DL tube, two pouches of sucti |
| 07290013745590 | Visualized double lumen endobronchial tube set. the set contains 1 DL tube + two pouches of suct |