Primary Device ID | 17350046131443 |
NIH Device Record Key | 3336f196-8aff-440e-ba76-c55e59a7971a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NomoLine™ HH Adult Single Nasal Prong CO2 Cannula |
Version Model Number | 3839 |
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 | 07350046131446 [Unit of Use] |
GS1 | 17350046131443 [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 |