Primary Device ID | 00864974000257 |
NIH Device Record Key | b5e8a428-7008-44d3-8157-216d7d8e9c6f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Corridor4DM |
Version Model Number | v2018 |
Company DUNS | 621360762 |
Company Name | INVIA LLC |
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 | 00864974000257 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2018-09-01 |
00864974000257 | v2018 |
00864974000233 | v2017 |
00864974000226 | v2016 |
00864974000219 | v2015 |
00864974000202 | v2013 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CORRIDOR4DM 77506442 3569741 Live/Registered |
INVIA LLC 2008-06-24 |