| Primary Device ID | 00842000100652 |
| NIH Device Record Key | fd32fffe-d39c-45b0-9c6f-6a83dc328179 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | eFilm Workstation |
| Version Model Number | 4.2.1 |
| Company DUNS | 065626069 |
| Company Name | MERGE HEALTHCARE SOLUTIONS INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | 00842000100652 [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 | 2017-10-31 |
| 00842000100652 | 4.2.1 |
| 00842000100287 | Standalone software application |
| 00842000100850 | Standalone software application |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EFILM WORKSTATION 77335593 3563272 Live/Registered |
Merge Healthcare Incorporated 2007-11-21 |