Elekta Unity QA Lok-Bar™ MTULB002

GUDID 00841439113226

Non-conductive

MEDTEC, INC.

Indexed-immobilization patient positioning system

• Primary Device ID: 00841439113226
• NIH Device Record Key: cda05947-19f2-4665-9d48-f71633b9cb63
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Elekta Unity QA Lok-Bar™
• Version Model Number: MTULB002
• Catalog Number: MTULB002
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439113226 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-17
• Device Publish Date: 2020-08-09

Devices Manufactured by MEDTEC, INC.

• 00841439115039 - Posi Indexing Bar: 2025-01-10 For use with MTM3303, MTM3304, MTM3305, MTM3004
• 00841439114858 - Headrest - TIMO Size A, B, C, D, E, F: 2024-12-12 (19.8 x 12.2 x 6.4cm) size A; (22.6 x 11.9 x 6.4cm) size B; (23.1 x 11.7 x 7.4cm) size C; (23.4 x 12.4 x 8.9cm) size D; (21.8 x
• 00841439114865 - Headrest - Timo Size A: 2024-12-12 (19.8 x 12.2 x 6.4cm)
• 00841439114872 - Headrest - Timo size B: 2024-12-12 (22.6 x 11.9 x 6.4cm)
• 00841439114889 - Headrest - Timo size C: 2024-12-12 (23.1 x 11.7 x 7.4cm)
• 00841439114896 - Headrest - Timo size D: 2024-12-12 (23.4 x 12.4 x 8.9cm)
• 00841439114902 - Headrest - Timo size E: 2024-12-12 (21.8 x 12.2 x 10.2cm)
• 00841439114919 - Headrest - Timo Size F: 2024-12-12 (23.4 x 12.2 x 9.1cm)