Circulaire II Hybrid Aerosol Drug Delivery System

GUDID 10709078000833

Reusable VixOne, Mouthpiece, Filter

WESTMED, INC.

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• Primary Device ID: 10709078000833
• NIH Device Record Key: 249179a9-a1ef-43dc-88ce-452e5845f2bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Circulaire II Hybrid Aerosol Drug Delivery System
• Version Model Number: 0391R
• 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: false
• 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	00709078000836 [Primary]
GS1	10709078000833 [Package]; Contains: 00709078000836; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K926055

FDA Product Code

• CAF: Nebulizer (Direct Patient Interface)

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: 2016-12-16

On-Brand Devices [Circulaire II Hybrid Aerosol Drug Delivery System]

• 10709078000864: With VixOne, Mouthpiece, Filter
• 10709078000833: Reusable VixOne, Mouthpiece, Filter
• 10709078000819: with reusable VixOne, Mouthpiece