GUDID 20681490032142

VENT TUBE 1056165 5PK PLAIN FLPL .89X7

MEDTRONIC XOMED, INC.

Tympanostomy tube

• Primary Device ID: 20681490032142
• NIH Device Record Key: 93e03151-e8d2-49ac-bba0-0cdd1fdae489
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 1056165
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Length: 7 Millimeter
• Length: 7 Millimeter
• Length: 7 Millimeter
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter
• Device Size Text, specify: 0
• Length: 7 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681490032148 [Primary]
GS1	20681490032142 [Package]; Contains: 00681490032148; Package: PK [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151067

FDA Product Code

• ETD: TUBE, TYMPANOSTOMY

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-07-13

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