FDA UDI In Commercial Distribution 🇺🇸 United States

AcuityPDR

DI: 00810035220270 · Model: Standard · RADMEDIX, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AcuityPDR
Primary DI
00810035220270
Version / Model
Standard
Company Name
RADMEDIX, LLC
Labeler DUNS
005057263
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-04
Public Version
1
Public Version Date
2020-05-12
Public Version Status
New
Public Device Record Key
f4191df7-e46d-43cc-9d0c-d3bbcb33b702

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
IZL System, X-Ray, Mobile

GMDN Terms

Code Name
37643 Portable basic diagnostic x-ray system, digital

Identifiers

Type ID
Primary 00810035220270

Premarket Submissions

Submission Number Supplement Number
K200726 000