72" Adult Anesthesia Circuit

GUDID 10709078009638

72" Adult Anesthesia Circuit, GSE W/ Cap, Parallel WYE, 3L Not made with Latex Bag

WESTMED, INC.

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• Primary Device ID: 10709078009638
• NIH Device Record Key: 741abfeb-6306-4e03-a4fb-13f84fc718f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 72" Adult Anesthesia Circuit
• Version Model Number: 9165
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078009631 [Primary]
GS1	10709078009638 [Package]; Contains: 00709078009631; Package: [20 Units]; In Commercial Distribution

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

On-Brand Devices [72" Adult Anesthesia Circuit]

• 10709078009638: 72" Adult Anesthesia Circuit, GSE W/ Cap, Parallel WYE, 3L Not made with Latex Bag
• 10709078009553: 72" Adult Anesthesia Circuit, Expandable, plain elbow, parallel WYE w/GSP, 3L not made with late