Interloc® Lok-Bar™ MTM340525

GUDID 00841439106815

53cm

MEDTEC, INC.

Indexed-immobilization patient positioning system

• Primary Device ID: 00841439106815
• NIH Device Record Key: df2613e0-684a-4b1b-b38a-429d0f4bbfae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Interloc® Lok-Bar™
• Version Model Number: MTM340525
• Catalog Number: MTM340525
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00841439106815 [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

On-Brand Devices [Interloc® Lok-Bar™]

• 00841439110263: (50cm)
• 00841439106815: 53cm
• 00841439104873: (48cm)
• 00841439104842: (53cm)
• 00841439104835: (50cm)
• 00841439104828: (53cm)
• 00841439104712: (53cm)
• 00841439104705: (53cm)
• 00841439104675: (49.5cm)