Anesthesia Circuits

GUDID 10709078004336

Disposable Anesthesia Circuits, Adult 108"

WESTMED, INC.

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• Primary Device ID: 10709078004336
• NIH Device Record Key: b72c5aaf-1b81-4a65-925b-6a7bff377d7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anesthesia Circuits
• Version Model Number: 8143
• 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	00709078004339 [Primary]
GS1	10709078004336 [Package]; Contains: 00709078004339; Package: [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K922492

FDA Product Code

• CAH: Filter, Bacterial, Breathing-Circuit

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-27
• Device Publish Date: 2017-08-31

On-Brand Devices [Anesthesia Circuits]

• 10709078004374: Disposable Anesthesia Circuits, Adult 60"
• 00709078004346: Disposable Anesthesia Breathing Circuits, Adult 60"
• 10709078004336: Disposable Anesthesia Circuits, Adult 108"