FUSE

GUDID 00350227300040

FUSE version 1.06

PATTERSON TECHNOLOGY CENTER

Radiology PACS software

• Primary Device ID: 00350227300040
• NIH Device Record Key: 3a35e294-9bb8-484f-8048-4229f3a6c2e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FUSE
• Version Model Number: 1.06
• Company DUNS: 062232311
• Company Name: PATTERSON TECHNOLOGY CENTER
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00350227300040 [Primary]

FDA Product Code

• LLZ: System, Image Processing, Radiological

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: 2019-11-09

On-Brand Devices [FUSE]

• 00350227300026: FUSE version 1.02
• 00350227300019: FUSE version 1.01
• 00350227300002: Fuse version 1.00
• 00350227000223: FUSE version 1.04
• 00350227300040: FUSE version 1.06
• 00350227300057: FUSE version 1.07
• 00350227300033: FUSE version 1.05
• 00350227000216: FUSE version 1.03
• 00350227300071: FUSE version 1.09
• 00350227300064: FUSE version 1.08