Primary Device ID | 00842000100751 |
NIH Device Record Key | c325bfb3-0762-41d6-ad6f-4cd9ebdf34bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Merge Cardio V11.1 |
Version Model Number | 11.1 |
Company DUNS | 065626069 |
Company Name | MERGE HEALTHCARE SOLUTIONS 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 | 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 | 00842000100751 [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 | 2 |
Public Version Date | 2019-05-09 |
Device Publish Date | 2019-04-17 |
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00842000101086 - Merge PACS | 2023-09-22 |
00842000101130 - Merge Universal Viewer | 2023-09-07 |
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00842000101093 - Merge Universal Viewer | 2023-03-27 |