IRMA™ AX+

GUDID 07350046131712

Masimo Sweden AB

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• Primary Device ID: 07350046131712
• NIH Device Record Key: 6c3eea7d-d85b-41a1-92b8-7b355afcbf2f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IRMA™ AX+
• Version Model Number: AX+
• 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	07350046131712 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123043

FDA Product Code

• CBS: Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-11

On-Brand Devices [IRMA™ AX+]

• 07350046131736: AX+ LEMO
• 07350046131729: AX+ Bluepoint
• 07350046131712: AX+