| Primary Device ID | 00606959022287 |
| NIH Device Record Key | 6b2ea4cd-477d-43ed-84a5-14df40f7a650 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | COMFORTGEL BLUE FULL |
| Version Model Number | 00 |
| Catalog Number | 1081873 |
| Company DUNS | 080728314 |
| Company Name | Respironics, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does n |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(724)744-2500 |
| respironics.service@philips.co |
| Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Storage Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00606959022287 [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 | 2018-08-20 |
| Device Publish Date | 2015-11-06 |
| 00606959022287 | Full Face mask |
| 00606959043947 | X-Large ComfortGel Blue Full SE, Japan |
| 00606959043930 | Large ComfortGel Blue Full SE, Japan |
| 00606959043923 | Medium ComfortGel Blue Full SE, Japan |
| 00606959043916 | Small ComfortGel Blue Full SE, Japan |
| 00606959043909 | X-Large ComfortGel Blue Full, Japan |
| 00606959043893 | Large ComfortGel Blue Full, Japan |
| 00606959043886 | Medium ComfortGel Blue Full, Japan |
| 00606959043879 | Small ComfortGel Blue Full, Japan |