Primary Device ID | 00840682109802 |
NIH Device Record Key | 6bd4977c-3e3b-41f4-b160-612d420c4fe7 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 3.0T PETMR CMA |
Company DUNS | 160032025 |
Company Name | GENERAL ELECTRIC COMPANY |
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 | 00840682109802 [Primary] |
OUO | Tomographic imager combining emission computed tomography with nuclear magnetic resonance |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-01 |
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00195278005502 - NA | 2020-08-24 |