| Primary Device ID | 00606959042025 |
| NIH Device Record Key | fafa1907-274a-482b-9af5-4aa7d6356b12 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DreamMapper Mobile App Android (EMEA) |
| Version Model Number | 2.5 |
| Catalog Number | 1128265 |
| Company DUNS | 080728314 |
| Company Name | Respironics, Inc. |
| 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 | 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.com | |
| Phone | +1(724)744-2500 |
| respironics.service@philips.com | |
| Phone | +1(724)744-2500 |
| respironics.service@philips.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00606959042025 [Primary] |
| OUG | Medical device data system |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-10-05 |
| 00606959051300 | DreamMapper Android EU Instance v 2.13 |
| 00606959048546 | DreamMapper Mobile App Android (EMEA) |
| 00606959042025 | DreamMapper Mobile Application Android (EMEA) |
| 00606959049901 | DreamMapper Android EU Instance v 2.11 |
| 00606959049062 | DreamMapper Android EU Instance v 2.10 |