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 |