IRMA™ CO2

GUDID 07350046131682

Masimo Sweden AB

Patient monitoring system module, carbon dioxide

• Primary Device ID: 07350046131682
• NIH Device Record Key: 0e1cb2dc-7ed6-423b-9cfc-81f8eac4208b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IRMA™ CO2
• Version Model Number: CO2 Bluepoint
• Company DUNS: 632369067
• Company Name: Masimo Sweden AB
• 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: false
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350046131682 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123043

FDA Product Code

• CCK: Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-01
• Device Publish Date: 2016-08-11

On-Brand Devices [IRMA™ CO2]

• 07350046131903: CO2 Spacelabs
• 07350046131705: CO2 LEMO
• 07350046131699: CO2 Breas
• 07350046131682: CO2 Bluepoint
• 07350046131675: CO2
• 07350046132122: CO2