FloEasy Co-Flo, Disposable Heated Humidified Circuit Kit

GUDID 10709078004411

WESTMED, INC.

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• Primary Device ID: 10709078004411
• NIH Device Record Key: 4530c0de-fa8e-4063-8cad-6cec06524fcc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FloEasy Co-Flo, Disposable Heated Humidified Circuit Kit
• Version Model Number: 9571
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078004414 [Primary]
GS1	10709078004411 [Package]; Contains: 00709078004414; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K922492

FDA Product Code

• OFP: Anesthesia Breathing Circuit Kit (Adult & Pediatric)

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: 2017-09-07

On-Brand Devices [FloEasy Co-Flo, Disposable Heated Humidified Circuit Kit]

• 10709078004428: 9572
• 10709078004411: 9571