| Primary Device ID | 17350046131108 |
| NIH Device Record Key | 48c83f00-a830-4c5f-b12e-a1f4b033ed0c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NomoLine™ Pediatric Nasal CO2 Cannula with Luer |
| Version Model Number | 3805 |
| Company DUNS | 632369067 |
| Company Name | Masimo Sweden AB |
| Device Count | 25 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07350046131101 [Unit of Use] |
| GS1 | 17350046131108 [Primary] |
| CCK | Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase |
| 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 | 2017-12-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NOMOLINE 86185529 5418472 Live/Registered |
Masimo Corporation 2014-02-05 |