Rectangular Extension MTIL6660

GUDID 00841439106402

Reusable rectangular extension for use with Universal Couchtop™ Long Extension

MEDTEC, INC.

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• Primary Device ID: 00841439106402
• NIH Device Record Key: f34796f3-f0ff-4256-ab14-ff7b31c1e728
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rectangular Extension
• Version Model Number: MTIL6660
• Catalog Number: MTIL6660
• 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: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch
• Width: 20.9 Inch
• Length: 55.3 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439106402 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180021

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: 4
• Public Version Date: 2019-05-30
• Device Publish Date: 2017-08-02

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