Primary Device ID | 00857534006363 |
NIH Device Record Key | 860ad047-68db-4a07-be5e-5164df1037d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VISIUSmatrix |
Version Model Number | 115407-000 |
Company DUNS | 079990922 |
Company Name | DEERFIELD IMAGING, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 00857534006363 [Primary] |
LMD | System, Digital Image Communications, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-14 |
Device Publish Date | 2024-10-04 |
00857534006646 | Applications Platform 4.0 US/JPN – INT KIT – 3 Room 120087-000 |
00857534006639 | Applications Platform 4.0 US/JPN – INT KIT-120085-000 |
00857534006622 | Applications Platform 4.0 US/JPN – 3 Room- 119897-000 |
00857534006493 | Applications Platform 4.0 NA/JAPAN 2-Room- 119407-000 |
00857534006684 | Applications Platform 4.0 INTL – INT KIT – 3 Room |
00857534006677 | Applications Platform 4.0 INTL – INT KIT |
00857534006660 | Applications Platform 4.0 INTL – 3 Room |
00857534006653 | Applications Platform 4.0-INTL-2-Room |
00857534006363 | Application Platform 2.4 NA |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VISIUSMATRIX 97396750 not registered Live/Pending |
Deerfiled Imaging, Inc. 2022-05-05 |
VISIUSMATRIX 85427928 4771049 Live/Registered |
DEERFIELD IMAGING HOLDINGS, INC. 2011-09-21 |