| Primary Device ID | 00606959042001 |
| NIH Device Record Key | 6d98f57d-92c3-4f51-a39b-a39703048fe4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DreamMapper Web (EMEA) |
| Version Model Number | 2.5 |
| Catalog Number | 1128262 |
| 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 | 00606959042001 [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 |
| 00606959051263 | DreamMapper Web EU Instance v 2.13 |
| 00606959048515 | DreamMapper Web (EMEA) |
| 00606959042001 | DreamMapper Web (EMEA) |
| 00606959049864 | DreamMapper Web EU Instance v 2.11 |
| 00606959054851 | DreamMapper Web EU Instance, Version 2.18 |
| 00606959053519 | DreamMapper Web EMEA Instance v 2.16 |
| 00606959049031 | DreamMapper Web EU Instance v 2.10 |