| Primary Device ID | 00606959048553 | 
| NIH Device Record Key | 60858cce-3fb8-4027-9656-5a8e06a5f762 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | DreamMapper Mobile App Android (APAC) | 
| Version Model Number | 2.9 | 
| Catalog Number | 1127960 | 
| 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 | 00606959048553 [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 | 
| 00606959051317 | DreamMapper Android APAC Instance v 2.13 | 
| 00606959048553 | DreamMapper Mobile App Android (APAC) | 
| 00606959049918 | DreamMapper Android APAC Instance v 2.11 | 
| 00606959049079 | DreamMapper Android APAC Instance v 2.10 |