Eonis 19” K9356033A1X

GUDID 05415334045767

MDRC-1419 HNIB

Barco NV

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Primary Device ID05415334045767
NIH Device Record Key8bfd27a8-99bd-43a7-9efe-7505ae1d832b
Commercial Distribution StatusIn Commercial Distribution
Brand NameEonis 19”
Version Model NumberMDRC-1419
Catalog NumberK9356033A1X
Company DUNS371618773
Company NameBarco NV
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com
Phone+1 866-302-7939
Emailservice.medical.usa@barco.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105415334045767 [Primary]

FDA Product Code

LMDSystem, Digital Image Communications, Radiological

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-03
Device Publish Date2023-09-25

On-Brand Devices [Eonis 19”]

05415334045767MDRC-1419 HNIB
05415334045750MDRC-1419 HNIB CHH
05415334045743MDRC-1419 SNIB
05415334045736MDRC-1419 SNIB DIN
05415334045729MDRC-1419 STIB

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