FDA UDI In Commercial Distribution 🇺🇸 United States

miPlatform

DI: 06970901070010 · Model: V2.0 · Hinacom Software and Technology, Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
miPlatform
Primary DI
06970901070010
Version / Model
V2.0
Company Name
Hinacom Software and Technology, Ltd.
Labeler DUNS
421337255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-21
Public Version
5
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
4c25816e-4ca3-47ca-8ee4-18370c83693b

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LLZ System, Image Processing, Radiological

GMDN Terms

Code Name
41670 Radiological PACS software

Identifiers

Type ID
Primary 06970901070010