Interloc® Lok-Bar™ MTIL3152

GUDID 00841439104712

(53cm)

MEDTEC, INC.

Indexed-immobilization patient positioning system

• Primary Device ID: 00841439104712
• NIH Device Record Key: 2679a726-de43-4317-9270-9b9c149c1466
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Interloc® Lok-Bar™
• Version Model Number: MTIL3152
• Catalog Number: MTIL3152
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439104712 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K973842

FDA Product Code

• IXQ: Table, radiographic, stationary top

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-05-31
• 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)