TraumaCad Mobile

GUDID 07290109942001

BRAINLAB LTD

Radiology picture archiving and communication system application software

• Primary Device ID: 07290109942001
• NIH Device Record Key: 39d1859d-df1c-4e2f-bc9d-fbd4a049e6a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TraumaCad Mobile
• Version Model Number: 2.0
• Company DUNS: 533769907
• Company Name: BRAINLAB LTD
• Device Count: 1
• DM Exempt: false
• 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: false
• 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(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com
• Phone: +1(800)597-5911
• Email: us.support@brainlab.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109942001 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160001

FDA Product Code

• LLZ: System, Image Processing, Radiological

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: 2018-09-24
• Device Publish Date: 2016-09-23

Devices Manufactured by BRAINLAB LTD

• 07290109943015 - TraumaCad Neo: 2025-07-24
• 07290109943008 - TraumaCad Neo: 2024-01-01
• 07290109941004 - TraumaCad: 2018-09-24
• 07290109942001 - TraumaCad Mobile: 2018-09-24
• 07290109942001 - TraumaCad Mobile: 2018-09-24