Primary Device ID | 00842000100775 |
NIH Device Record Key | 2d7ba5a9-e064-4e5a-92a5-bf8fae22da99 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Merge OrthoPACS |
Version Model Number | 8.0 |
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 | false |
OTC Over-The-Counter | false |