Varian Mobius 3D

GUDID 00899475002431

VARIAN MEDICAL SYSTEMS, INC.

Radiation therapy software

• Primary Device ID: 00899475002431
• NIH Device Record Key: bfc72cfd-d99b-4cd5-a744-403039b3f392
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Varian Mobius 3D
• Version Model Number: 2.1
• Company DUNS: 035520894
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00899475002431 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153014

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: 2019-11-07
• Device Publish Date: 2019-10-30

Devices Manufactured by VARIAN MEDICAL SYSTEMS, INC.

• 00855141006349 - Eclipse Treatment Planning System: 2024-12-30
• 00856100006370 - ARIA Radiation Therapy Management: 2024-12-30
• 10856100006223 - Gating Reflector Block: 2024-12-11
• 00850800006074 - Vitesee: 2024-11-11
• 00858086006467 - Varian Collimator Accessories 30 CM wedge set lower (JITKIT): 2024-10-07
• 00858086006474 - Varian Collimator Accessories 30 CM wedge set upper (JITKIT): 2024-10-07
• 00858086006481 - Varian Collimator Accessories 20 cm wedge set lower: 2024-10-07
• 00858086006498 - Varian Collimator Accessories Lead wedge set lower (JITKIT): 2024-10-07