Primary Device ID | 05415334025981 |
NIH Device Record Key | 9d3c7da3-a566-47c1-b608-3bb2bb821399 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Coronis Fusion 4 MP |
Version Model Number | MDCC-4430 |
Catalog Number | K9301628A |
Company DUNS | 371618773 |
Company Name | Barco NV |
Device Count | 1 |
DM Exempt | true |
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 | 05415334025981 [Primary] |
PGY | Display, diagnostic radiology |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-31 |
Device Publish Date | 2020-07-23 |
05415334002340 | MDCC-4430 |
05415334028845 | MDCC-4430 MDT |
05415334025981 | MDCC-4430 NC |
05415334034785 | MDCC-4430 MDT MKII |