Cohen

GUDID 20763000040479

VENT TUBE 24701 5PK COHEN SILICONE

MEDTRONIC XOMED, INC.

Tympanostomy tube

• Primary Device ID: 20763000040479
• NIH Device Record Key: fb8213c9-d986-4baf-ad7a-311738393a1c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cohen
• Version Model Number: 24701
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter
• Length: 9.1 Millimeter
• Lumen/Inner Diameter: 1.14 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000040475 [Primary]
GS1	20763000040479 [Package]; Contains: 00763000040475; 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: 2020-05-19
• Device Publish Date: 2020-05-11

On-Brand Devices [Cohen]

• 20681490063474: VENT TUBE 25691 MICROGEL 5PK COHEN 1.14
• 20681490062880: VENT TUBE 24701 5PK COHEN SILICONE
• 20763000040479: VENT TUBE 24701 5PK COHEN SILICONE