Varian IDENTIFY

GUDID 00899475002592

VARIAN MEDICAL SYSTEMS, INC.

Real-time position management respiratory gating system, optical

• Primary Device ID: 00899475002592
• NIH Device Record Key: 5f9f0869-7d69-48d9-b922-eda4530775ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Varian IDENTIFY
• Version Model Number: 2.2
• Company DUNS: 009120817
• Company Name: VARIAN MEDICAL SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	00899475002592 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192968

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: 2019-11-25
• Device Publish Date: 2019-11-16

Devices Manufactured by VARIAN MEDICAL SYSTEMS, INC.

• 00857235006082 - Halcyon: 2026-02-03
• 00857235006105 - Ethos Radiotherapy System: 2026-02-03
• 00858086006771 - TrueBeam: 2026-01-23
• 00858086006788 - VitalBeam: 2026-01-23
• 00858086006795 - EDGE: 2026-01-23
• 00858086006825 - TrueBeam STx: 2026-01-23
• 00899475002110 - High-Definition 120 Multileaf Collimator: 2026-01-14
• 00857235006075 - Halcyon: 2026-01-13