IMRISeye

GUDID 00857534006752

IMRISeye

DEERFIELD IMAGING, INC.

Radiological general body-part positioner

• Primary Device ID: 00857534006752
• NIH Device Record Key: d3f9ab5d-0c6c-4e95-829d-9f4c25e6fd7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMRISeye
• Version Model Number: 120783-000
• Company DUNS: 079990922
• Company Name: DEERFIELD IMAGING, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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	00857534006752 [Primary]

FDA Product Code

• FTY: Tape, Measuring, Rulers And Calipers

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: 2024-10-14
• Device Publish Date: 2024-10-04

On-Brand Devices [IMRISeye]

• 00857534006820: 120999-000
• 00857534006752: IMRISeye