IDENTIFY

GUDID 00858086006801

VARIAN MEDICAL SYSTEMS, INC.

Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical Real-time position management respiratory gating system, optical

• Primary Device ID: 00858086006801
• NIH Device Record Key: d1f2bcb6-20c6-49c5-a7e3-f615c86e0128
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IDENTIFY
• Version Model Number: 3.0
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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	00858086006801 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230576

FDA Product Code

• IYE: Accelerator, linear, 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: 2023-08-14
• Device Publish Date: 2023-08-04

On-Brand Devices [IDENTIFY]

• 00856100006240: 2.3
• 00858086006801: 3.0