Primary Device ID | 00840682141994 |
NIH Device Record Key | 193a107f-4b79-49f3-806b-4069b9c1ca82 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Discovery MI Columbird mE2 Application SW |
Version Model Number | 2.0 |
Company DUNS | 809785715 |
Company Name | GE MEDICAL SYSTEMS, 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 | true |
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 | 00840682141994 [Primary] |
KPS | System, tomography, computed, emission |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-03 |
Device Publish Date | 2018-08-03 |
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