VISIUSmatrix

GUDID 00857534006646

Applications Platform 4.0 US/JPN – INT KIT – 3 Room 120087-000

DEERFIELD IMAGING, INC.

Operating room audiovisual data/device management system application software

• Primary Device ID: 00857534006646
• NIH Device Record Key: 0bfd3590-49c9-4b62-b513-dc417fa278cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VISIUSmatrix
• Version Model Number: Application Platform 4.0 KIT
• Company DUNS: 079990922
• Company Name: DEERFIELD IMAGING, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857534006646 [Primary]

FDA Product Code

• LMD: System, Digital Image Communications, 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: 2020-09-23
• Device Publish Date: 2020-09-15

On-Brand Devices [VISIUSmatrix]

• 00857534006646: Applications Platform 4.0 US/JPN – INT KIT – 3 Room 120087-000
• 00857534006639: Applications Platform 4.0 US/JPN – INT KIT-120085-000
• 00857534006622: Applications Platform 4.0 US/JPN – 3 Room- 119897-000
• 00857534006493: Applications Platform 4.0 NA/JAPAN 2-Room- 119407-000
• 00857534006684: Applications Platform 4.0 INTL – INT KIT – 3 Room
• 00857534006677: Applications Platform 4.0 INTL – INT KIT
• 00857534006660: Applications Platform 4.0 INTL – 3 Room
• 00857534006653: Applications Platform 4.0-INTL-2-Room
• 00857534006363: Application Platform 2.4 NA