Circulaire

GUDID 10709078009133

Circulaire Aerosol Masks

WESTMED, INC.

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• Primary Device ID: 10709078009133
• NIH Device Record Key: e67e6490-2805-4773-ac1d-86c56e6a89a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Circulaire
• Version Model Number: 0290
• 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	00709078009136 [Primary]
GS1	10709078009133 [Package]; Contains: 00709078009136; Package: [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K926055

FDA Product Code

• BYG: Mask, Oxygen

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-08
• Device Publish Date: 2020-08-31

On-Brand Devices [Circulaire]

• 10709078009140: Circulaire Aerosol Masks
• 10709078009133: Circulaire Aerosol Masks