Armstrong V

GUDID 20763000039480

VENT TUBE 1056121 5PK ARMSTR V 1.14X4.5

MEDTRONIC XOMED, INC.

Tympanostomy tube

• Primary Device ID: 20763000039480
• NIH Device Record Key: cdef7179-bcd9-4f6c-8d60-d2c17cee486d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Armstrong V
• Version Model Number: 1056121
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

Device Dimensions

• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 4.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000039486 [Primary]
GS1	20763000039480 [Package]; Contains: 00763000039486; 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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-01
• Device Publish Date: 2020-04-23

On-Brand Devices [Armstrong V]

• 20681490032623: VENT TUBE 1066121 10PK ARMST PR 1.14X4.5
• 20681490032616: VENT TUBE 1066120 10PK ARMSTRNG V PAIR
• 20681490032500: VENT TUBE 1066033 10PK ARMSTNG V GROM PR
• 20681490032067: VENT TUBE 1056121 5PK ARMSTR V 1.14X4.5
• 20681490032050: VENT TUBE 1056120 5PK ARMSTR V 1.14X7.5
• 20681490031879: VENT TUBE 1056033 5PK ARMSTR V GROMMET
• 20681490031855: VENT TUBE 1056031 5PK ARMSTRG V 1.14X4.5
• 20763000039480: VENT TUBE 1056121 5PK ARMSTR V 1.14X4.5
• 20763000039473: VENT TUBE 1056120 5PK ARMSTR V 1.14X7.5