Primary Device ID | 00195278630384 |
NIH Device Record Key | 0022bab6-2fe4-4ed6-bbee-dfffaaabf3d1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spectral Color Overlay |
Version Model Number | 1.0 |
Catalog Number | 5929649 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00195278630384 [Primary] |
JAK | System, x-ray, tomography, computed |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-04 |
Device Publish Date | 2023-08-25 |
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