FDA UDI In Commercial Distribution 🇺🇸 United States

Radmedix

DI: 00810035220065 · Model: AcuitySDR+ · RADMEDIX, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Radmedix
Primary DI
00810035220065
Version / Model
AcuitySDR+
Company Name
RADMEDIX, LLC
Labeler DUNS
005057263
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-27
Public Version
1
Public Version Date
2020-03-06
Public Version Status
New
Public Device Record Key
995f6761-0c49-430d-958d-b1637ed8c603

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
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
Yes
Sterilization Methods
Liquid Chemical

Product Codes

Code Name
KPR System, X-Ray, Stationary

GMDN Terms

Code Name
37645 Stationary basic diagnostic x-ray system, digital

Identifiers

Type ID
Primary 00810035220065

Premarket Submissions

Submission Number Supplement Number
K193360 000