iMRI 3T S

GUDID 00857534006059

IMRIS SSK OR-DR Partial Body Imaging, 116118-000

DEERFIELD IMAGING, INC.

Full-body MRI system, superconducting magnet

• Primary Device ID: 00857534006059
• NIH Device Record Key: 26034910-eb21-4ad1-a1cc-5840d8ce9ca1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iMRI 3T S
• Version Model Number: OR-DR, 116118-000
• Company DUNS: 079990922
• Company Name: DEERFIELD IMAGING, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	00857534006059 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133692

FDA Product Code

• LNH: System, Nuclear Magnetic Resonance Imaging

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: 2018-07-06
• Device Publish Date: 2016-09-19

On-Brand Devices [iMRI 3T S]

• 00857534006066: IMRIS SSK OR-DR Full Body Imaging, 116119-000
• 00857534006059: IMRIS SSK OR-DR Partial Body Imaging, 116118-000
• 00857534006042: IMRIS SSK OR-DR-OR Full Body Imaging,116117-000
• 00857534006035: IMRIS SSK OR-DR-OR Partial Body Imaging, 116053-000