Primary Device ID | 00860148000832 |
NIH Device Record Key | 5d0cffc8-df5f-4465-b69c-35c3cf70dfdd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mobile MIM |
Version Model Number | 4.1 |
Company DUNS | 136977290 |
Company Name | MIM SOFTWARE INC. |
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 | 00860148000832 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-01 |
Device Publish Date | 2019-10-24 |
00865936000216 | A mobile medical imaging software package that is used for the viewing, registration, fusion, an |
00860148000832 | A mobile medical imaging software package that is used for the viewing, registration, fusion, an |
00860148000894 | A mobile medical imaging software package that is used for the viewing, registration, fusion, an |