Primary Device ID | 00863039000423 |
NIH Device Record Key | dfa1105e-8d09-44cb-86aa-c3e21503c690 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prosomnus IA MicrO2 |
Version Model Number | MicrO2 |
Company DUNS | 075438768 |
Company Name | PROSOMNUS SLEEP TECHNOLOGIES |
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 | true |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00863039000423 [Primary] |
LRK | Device, Anti-Snoring |
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 | 2017-06-21 |
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00863039000409 - Prosomnus CA Sleep and Snore Device | 2018-07-06 |
00863039000416 - Prosomnus IA Monogram | 2018-07-06 Device for Obstructive Sleep Apnea iterative adjustment with patient comfort features |
00863039000423 - Prosomnus IA MicrO2 | 2018-07-06Obstructive Sleep Apnea Device with twin mated posts |
00863039000423 - Prosomnus IA MicrO2 | 2018-07-06 Obstructive Sleep Apnea Device with twin mated posts |
00863039000430 - Prosomnus IA with Patient Monitoring | 2018-07-06 Obstructive Sleep Apnea with Iterative Adjustment and Patient Monitoring |