FDA UDI In Commercial Distribution 🇺🇸 United States

iMRX System

DI: 00857534006165 · Model: iMRX System AR-DR-OR · DEERFIELD IMAGING, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iMRX System
Primary DI
00857534006165
Version / Model
iMRX System AR-DR-OR
Company Name
DEERFIELD IMAGING, INC.
Labeler DUNS
079990922
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-04
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a20d3718-831f-463e-9c1e-c83d767d1866

Device Description

iMRX System AR-DR-OR, MR30R, 105828-000

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

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 00857534006165

Premarket Submissions

Submission Number Supplement Number
K101813 000