| Primary Device ID | 00865936000216 |
| NIH Device Record Key | 6b59b6b8-231d-437e-af21-e97c99bb269f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mobile MIM |
| Version Model Number | 4.0 |
| 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 | 00865936000216 [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 | 4 |
| Public Version Date | 2019-05-23 |
| Device Publish Date | 2016-10-25 |
| 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 |