Westaby T-Y Stent

GUDID 00815347022550

Hood Bifurcated T-Tube

HOOD, E BENSON LABORATORIES INC

Basic tracheostomy tube, single-use

• Primary Device ID: 00815347022550
• NIH Device Record Key: 458c6bf5-0a1a-4f78-af36-e43f8dea4f96
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Westaby T-Y Stent
• Version Model Number: RTY-14-S
• Company DUNS: 076603380
• Company Name: HOOD, E BENSON LABORATORIES INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	00815347022550 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K864533

FDA Product Code

• BTO: Tube, Tracheostomy (W/Wo Connector)

Sterilization

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

[00815347022550]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00815347022550]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00815347022550]

Moist Heat or Steam Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-12-21

On-Brand Devices [Westaby T-Y Stent]

• 00815347022567: Hood Bifurcated T-Tube
• 00815347022550: Hood Bifurcated T-Tube
• 00815347022543: Hood Bifurcated T-Tube
• 00815347022536: Hood Bifurcated T-Tube