FDA UDI In Commercial Distribution 🇺🇸 United States

iMRX System

DI: 00857534006189 · Model: iMRX System AR-DR MR30RS · DEERFIELD IMAGING, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iMRX System
Primary DI
00857534006189
Version / Model
iMRX System AR-DR MR30RS
Company Name
DEERFIELD IMAGING, INC.
Labeler DUNS
079990922
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b2b1d540-2322-403c-9c66-77cc6fdbf3bb

Device Description

iMRX System AR-DR MR30RS,105824-000

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IZI System, X-Ray, Angiographic
LNH System, Nuclear Magnetic Resonance Imaging

GMDN Terms

Code Name
37654 Full-body MRI system, superconducting magnet
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 00857534006189

Premarket Submissions

Submission Number Supplement Number
K101813 000