InLine Water Trap

GUDID 10709078014069

Inline Water Trap For Oxygen Delivery

WESTMED, INC.

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• Primary Device ID: 10709078014069
• NIH Device Record Key: bd58dfd8-12b4-49d7-a31d-70a531031083
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InLine Water Trap
• Version Model Number: 1002277
• 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: false
• Serial Number: true
• 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	00709078014062 [Primary]
GS1	10709078014069 [Package]; Contains: 00709078014062; Package: [25 Units]; In Commercial Distribution

FDA Product Code

• CAW: Generator, Oxygen, Portable

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: 2022-04-08
• Device Publish Date: 2022-03-31

On-Brand Devices [InLine Water Trap]

• 00709078002601: Inline Water Trap, For Oxygen Delivery (This is a component of the Composite Kit for Nationwide
• 10709078014069: Inline Water Trap For Oxygen Delivery