Hunsaker

GUDID 00681490156431

VENTILATION TUBE 7080100 HUNSAKR MON-JET

MEDTRONIC XOMED, INC.

High-frequency ventilation endotracheal tube

• Primary Device ID: 00681490156431
• NIH Device Record Key: 65fc044e-4ca5-4915-8777-8f4343cea8c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hunsaker
• Version Model Number: 7080100
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681490156431 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K922880

FDA Product Code

• BTR: Tube, tracheal (w/wo connector)

Sterilization

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

Device Entry Metadata

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

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