Inline Water Trap

GUDID 00709078002601

Inline Water Trap, For Oxygen Delivery (This is a component of the Composite Kit for Nationwide Home Med - Part #0837)

WESTMED, INC.

Breathing circuit condensate trap, reusable Breathing circuit condensate trap, reusable

• Primary Device ID: 00709078002601
• NIH Device Record Key: d0d26c6d-aad4-4fcc-823e-d06451c580cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Inline Water Trap
• Version Model Number: 0221B
• 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	00709078002601 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K954271

FDA Product Code

• CAW: Generator, Oxygen, Portable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-04-19

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