Body Pro-Lok™ Patient Transfer Base MTSBRT012

GUDID 00841439107324

Body Pro-Lok™ Patient Transfer Base

MEDTEC, INC.

Patient transfer sliding board

• Primary Device ID: 00841439107324
• NIH Device Record Key: e6667ffd-1e89-4e63-8698-e6da46e1a117
• Commercial Distribution Discontinuation: 2020-02-08
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Body Pro-Lok™ Patient Transfer Base
• Version Model Number: MTSBRT012
• Catalog Number: MTSBRT012
• 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	00841439107324 [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

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