Primary Device ID | 07340024700030 |
NIH Device Record Key | 04c739fb-a81b-4ce5-9ffc-66796ca4f003 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SyMRI |
Version Model Number | 11 |
Company DUNS | 775572188 |
Company Name | SyntheticMR AB (publ) |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07340024700030 [Primary] |
LNH | System, Nuclear Magnetic Resonance Imaging |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-07-23 |
Device Publish Date | 2018-06-20 |
07340024700030 | SyMRI is a post-processing software medical device intended for use in visualization of the brai |
07340024700023 | SyMRI is a post-processing software medical device intended for use in visualization of the brai |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SYMRI 85974094 4661808 Live/Registered |
Synthetic MR AB (publ) 2013-07-01 |