Spacer 107104MR

GUDID 00841439114636

30mm spacer, MR

MEDTEC, INC.

Radiological headrest Radiological headrest Radiological headrest

• Primary Device ID: 00841439114636
• NIH Device Record Key: 0a6e306e-07cc-4b89-b57b-659a43ee8617
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spacer
• Version Model Number: 107104MR
• Catalog Number: 107104MR
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439114636 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180021

FDA Product Code

• IYE: Accelerator, linear, medical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-17
• Device Publish Date: 2024-07-09

On-Brand Devices [Spacer]

• 00841439111079: 30mm spacer
• 00841439111062: 20mm spacer
• 00841439114636: 30mm spacer, MR
• 00841439114629: 20mm spacer, MR