FUSE

GUDID 00350227300019

FUSE version 1.01

PATTERSON TECHNOLOGY CENTER

Radiology PACS software

• Primary Device ID: 00350227300019
• NIH Device Record Key: 390252be-8d54-47b0-9586-2f53e0b80092
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FUSE
• Version Model Number: 1.01
• 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	00350227300019 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-05-23
• Device Publish Date: 2018-05-07

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