Primary Device ID | 05415334000377 |
NIH Device Record Key | 24995d02-2b3e-414c-aa94-06f72505904d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nio Color 2MP |
Version Model Number | MDNC-2123 |
Catalog Number | K9300332A |
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 | 05415334000377 [Primary] |
PGY | Display, diagnostic radiology |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-19 |
Device Publish Date | 2017-12-07 |
05415334002029 | MDNC-2123 DE WP |
05415334002005 | MDNC-2221 EM |
05415334000384 | MDNC-2123 DE WH |
05415334000377 | MDNC-2123 EM BL |
05415334002623 | MDNC-2123 NEU MKII |
05415334002616 | MDNC-2123 EM BL MKII |
05415334002609 | MDNC-2123 DE WP MKII |
05415334002357 | MDNC-2123 DE WH MKII |
05415334032880 | MDNC-2521 SPES |
05415334032873 | MDNC-2521 SNES |
05415334043916 | MDNC-2123 DE WH |
05415334043763 | MDNC-2521 SNES |
05415334043749 | MDNC-2521 SPES |