Auto-Lok Assembly MTSBRT033

GUDID 00841439107386

Auto-Lok Assembly

MEDTEC, INC.

Patient transfer sliding board

• Primary Device ID: 00841439107386
• NIH Device Record Key: 41ae98ea-894c-45f5-8efe-e9d7f0157f6e
• Commercial Distribution Discontinuation: 2020-02-08
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Auto-Lok Assembly
• Version Model Number: MTSBRT033
• Catalog Number: MTSBRT033
• 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 Dimensions

• Length: 6.97 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439107386 [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: 6
• Public Version Date: 2020-02-10
• Device Publish Date: 2017-08-02

On-Brand Devices [Auto-Lok Assembly]

• 00841439107386: Auto-Lok Assembly
• 00841439107379: Auto-Lok Assembly