HumidX Plus

GUDID 00619498388110

Pack of 50

RESMED LIMITED

Heat/moisture exchanger insertable filter

• Primary Device ID: 00619498388110
• NIH Device Record Key: 71d24c37-f522-4c12-917f-5c09fbbf5e65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HumidX Plus
• Version Model Number: 38811
• Company DUNS: 751149311
• Company Name: RESMED LIMITED
• 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: 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00619498388110 [Primary]

FDA Product Code

• BYD: Condenser, Heat And Moisture (Artificial Nose)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-04-28

On-Brand Devices [HumidX Plus]

• 00619498388134: Humidx Plus 6PK
• 00619498388127: Humidx Plus 3PK
• 00619498388110: Pack of 50