Tubing

GUDID 10709078012652

Tubing, Corrugate, 10mm x 1' Clear

WESTMED, INC.

Anaesthesia breathing circuit, single-use

• Primary Device ID: 10709078012652
• NIH Device Record Key: 9f1c9cdf-0953-416c-abb2-4b2ca248bd70
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tubing
• Version Model Number: 0472
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 150
• 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	00709078012655 [Primary]
GS1	10709078012652 [Unit of Use]

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: 2021-07-08
• Device Publish Date: 2021-06-30

On-Brand Devices [Tubing]

• 10709078011440: Tubing, 10' KROT, W/Sleeves and Nuts, Vortran
• 10709078011518: Tubing, 20' KROT, Green, W/Sleeves and Nuts, Vortran
• 10709078012638: Tubing, Corrugate, Clear, 72" x 10mm
• 10709078012652: Tubing, Corrugate, 10mm x 1' Clear
• 10709078012928: Tubing, Corrugated 22mm X 120"