Primary Device ID | 00842000101147 |
NIH Device Record Key | f279d54f-fc7b-4f34-87f5-89ee61313a33 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Merge PACS |
Version Model Number | 9.1 |
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 | false |
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 | 00842000101147 [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 | 2023-12-06 |
Device Publish Date | 2023-11-28 |
00842000100737 | 8.0 |
00842000100690 | Merge PACS™ is a standards-based medical imaging diagnostic workstation that serves as an adju |
00842000100607 | Standalone software application |
00842000100560 | Standalone software application |
00842000100508 | Standalone software application |
00842000100409 | 7.2 |
00842000100072 | Standalone software application |
00842000100805 | 8.1 |
00842000100478 | 7.1.2.1 |
00842000100935 | 8.2 |
00842000101086 | 9.0 |
00842000101147 | 9.1 |
00842000101154 | 9.2 |