Mobius3D Mobius3D

GUDID 08613340003001

Secondary Check QA Software

VARIAN MEDICAL SYSTEMS, INC.

Accelerator system quality assurance device

• Primary Device ID: 08613340003001
• NIH Device Record Key: 93859f87-47a0-480b-923e-ca418b280561
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mobius3D
• Version Model Number: 2.0.1
• Catalog Number: Mobius3D
• Company DUNS: 009120817
• Company Name: VARIAN MEDICAL SYSTEMS, INC.
• 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: 888-263-8541
• Email: support@mobiusmed.com
• Phone: 888-263-8541
• Email: support@mobiusmed.com
• Phone: 888-263-8541
• Email: support@mobiusmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08613340003001 [Primary]

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: 3
• Public Version Date: 2020-05-19
• Device Publish Date: 2016-09-14

On-Brand Devices [Mobius3D]

• 08613340003001: Secondary Check QA Software
• 00861334000315: Secondary Check QA Software
• 00850800006043: 4.0