Primary Device ID | 00840682123532 |
NIH Device Record Key | f61b9e47-555c-4a59-b72e-dff4aac700cf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GE Client Software |
Version Model Number | v6.9.6 R3 |
Company DUNS | 784985108 |
Company Name | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, 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 | false |
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 |