Varian Verification Console

GUDID 00856104006123

VARIAN MEDICAL SYSTEMS INDIA SOFTWARE PRIVATE LIMITED

Radiation therapy treatment record/verify system

• Primary Device ID: 00856104006123
• NIH Device Record Key: 3eb2f067-3bb1-4606-93ad-4cff4cd15798
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Varian Verification Console
• Version Model Number: 2.3
• Company DUNS: 863318313
• Company Name: VARIAN MEDICAL SYSTEMS INDIA SOFTWARE PRIVATE LIMITED
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856104006123 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K124002

FDA Product Code

• LHN: System, radiation therapy, charged-particle, medical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-18
• Device Publish Date: 2019-11-08

On-Brand Devices [Varian Verification Console]

• 00856104006123: 2.3
• 00856104006079: 2.2