Varian Interface MTIL6610

GUDID 00841439106303

For use with Universal Couchtop™

MEDTEC, INC.

Indexed-immobilization patient positioning system

• Primary Device ID: 00841439106303
• NIH Device Record Key: 89890a93-cbfc-42f0-8f1e-86bc6a7c67fd
• Commercial Distribution Discontinuation: 2020-07-10
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Varian Interface
• Version Model Number: MTIL6610
• Catalog Number: MTIL6610
• Company DUNS: 103977526
• Company Name: MEDTEC, INC.
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com

Device Dimensions

• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter
• Width: 60.6 Centimeter
• Length: 60.8 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439106303 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K973842

FDA Product Code

• IXQ: Table, radiographic, stationary top

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-07-01
• Device Publish Date: 2017-08-02

On-Brand Devices [Varian Interface]

• 00841439106303: For use with Universal Couchtop™
• 00841439106327: Uc Varian Interface