Coil Support MTM340510

GUDID 00841439106808

Reusable non-sterile coil support for use with Philips Ingenia MR overlay

MEDTEC, INC.

Radiological whole-body positioner

• Primary Device ID: 00841439106808
• NIH Device Record Key: 8c64997e-4c7b-4f0d-a0f0-6bff6735b05d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Coil Support
• Version Model Number: MTM340510
• Catalog Number: MTM340510
• Company DUNS: 103977526
• Company Name: MEDTEC, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch
• Width: 17.4 Inch
• Length: 25.9 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439106808 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080072

FDA Product Code

• IYE: Accelerator, linear, medical

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: 2019-05-31
• Device Publish Date: 2017-08-02

On-Brand Devices [Coil Support]

• 00841439106778: For use with Philips Ingenia MR overlay
• 00841439106808: Reusable non-sterile coil support for use with Philips Ingenia MR overlay