| Primary Device ID | 00814747020708 |
| NIH Device Record Key | 834407cd-96f9-49e4-adb8-2edde3368251 |
| Commercial Distribution Discontinuation | 2019-02-21 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Ascend Full Face Vented Mask System |
| Version Model Number | 50825 |
| Company DUNS | 785635186 |
| Company Name | SLEEPNET, CORP. |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 1-800-742-3646 |
| xxx@xx.xx | |
| Phone | 1-800-742-3646 |
| xxx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00814747020708 [Primary] |
| BZD | Ventilator, Non-Continuous (Respirator) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-02-25 |
| Device Publish Date | 2016-07-05 |
| 00814747020708 | Full face vented mask for use in positive pressure ventilation. |
| 00814747021774 | Full face vented mask for use in positive pressure ventilation. |
| 00814747022504 | Full face vented mask for use in positive pressure ventilation. |
| 00814747022344 | Full face vented mask for use in positive pressure ventilation. |
| 00814747024225 | Full face vented mask for use in positive pressure ventilation. |
| 00814747024201 | Full face vented mask for use in positive pressure ventilation. |