| Primary Device ID | 00606959048508 |
| NIH Device Record Key | 4edf0e48-7136-43de-a322-7f05fa456ca3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DreamMapper Web (DM) |
| Version Model Number | 2.9 |
| Catalog Number | 1101679 |
| Company DUNS | 080728314 |
| Company Name | Respironics, Inc. |
| 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 | 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 | 00606959048508 [Primary] |
| MNT | VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-10-04 |
| 00606959051256 | DreamMapper Web NA Instance v 2.13 |
| 00606959048508 | DreamMapper Web |
| 00606959049857 | DreamMapper Web NA Instance v 2.11 |
| 00606959054844 | DreamMapper Web North American Instance, Version 2.18 |
| 00606959053045 | DreamMapper Web NA Instance v 2.15 |
| 00606959052093 | DreamMapper Web NA Instance v 2.14 |
| 00606959049024 | DreamMapper Web NA Instance v 2.10 |