Guide Pins 109036

GUDID 00841439100530

For use with Medical Intelligence Couchtop

MEDTEC, INC.

Indexed-immobilization patient positioning system

• Primary Device ID: 00841439100530
• NIH Device Record Key: 980e1acf-0b08-4de8-a15f-bbbc519a8a56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Pins
• Version Model Number: 109036
• Catalog Number: 109036
• 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: 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

Device Dimensions

• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter
• Length: 12 Centimeter
• Width: 2 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439100530 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K060737

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: 5
• Public Version Date: 2020-03-19
• Device Publish Date: 2017-08-02

On-Brand Devices [Guide Pins]

• 00841439101445: Reusable non-sterile Couchtop Fixation pieces (2)
• 00841439101421: Reusable non-sterile guide pins for use with Lok-bar
• 00841439100561: Reusable non-sterile guide pins for use with Medical Intelligence Couchtop
• 00841439100530: For use with Medical Intelligence Couchtop
• 00841439100462: For use with Varian Exact™ Couchtop