Template MTM340520

GUDID 00841439102534

For use with Philips Ingenia MR overlay

MEDTEC, INC.

Indexed-immobilization patient positioning system

• Primary Device ID: 00841439102534
• NIH Device Record Key: 249996e6-9cdb-48c5-a3ad-6473a52e94f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Template
• Version Model Number: MTM340520
• Catalog Number: MTM340520
• 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

Device Dimensions

• Length: 22 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439102534 [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: 2020-03-12
• Device Publish Date: 2017-08-02

Devices Manufactured by MEDTEC, INC.

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• 00841439114674 - Pronumbra: 2025-09-22 Pronumbra Helping Hand, Right
• 00841439114681 - Pronumbra: 2025-09-22 Pronumbra 130cm kVue
• 00841439114698 - Pronumbra: 2025-09-22 Pronumbra Neck Support, 40mm
• 00841439114704 - Pronumbra: 2025-09-22 Pronumbra Neck Support, 50mm
• 00841439114711 - Pronumbra: 2025-09-22 Pronumbra Neck Support, 65mm
• 00841439114728 - Pronumbra: 2025-09-22 Pronumbra Shoulder Adapter
• 00841439114841 - ZiFix Traverse: 2025-09-22 ZiFix Traverse with ONEClamp