Primary Device ID | 06970901070010 |
NIH Device Record Key | 4c25816e-4ca3-47ca-8ee4-18370c83693b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | miPlatform |
Version Model Number | V2.0 |
Company DUNS | 421337255 |
Company Name | Hinacom Software and Technology, Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06970901070010 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-09-24 |
Device Publish Date | 2017-06-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MIPLATFORM 98209300 not registered Live/Pending |
MiView Integrated Solutions, LLC 2023-10-04 |
![]() MIPLATFORM 86026911 4881987 Live/Registered |
Hinacom Software and Technology, Ltd. 2013-08-02 |