Primary Device ID | 05415334045767 |
NIH Device Record Key | 8bfd27a8-99bd-43a7-9efe-7505ae1d832b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Eonis 19” |
Version Model Number | MDRC-1419 |
Catalog Number | K9356033A1X |
Company DUNS | 371618773 |
Company Name | Barco NV |
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 | 05415334045767 [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 | 2023-10-03 |
Device Publish Date | 2023-09-25 |
05415334045767 | MDRC-1419 HNIB |
05415334045750 | MDRC-1419 HNIB CHH |
05415334045743 | MDRC-1419 SNIB |
05415334045736 | MDRC-1419 SNIB DIN |
05415334045729 | MDRC-1419 STIB |