McKesson Cardiology™

GUDID 80010939070018

MCKESSON TECHNOLOGIES INC.

Cardiology information system
Primary Device ID80010939070018
NIH Device Record Key6793dc68-bc85-4870-9659-26fbc899af73
Commercial Distribution StatusIn Commercial Distribution
Brand NameMcKesson Cardiology™
Version Model Number13.2.1
Company DUNS962049362
Company NameMCKESSON TECHNOLOGIES INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS180010939070018 [Primary]

FDA Product Code

LLZSystem, Image Processing, Radiological

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-08-30

Devices Manufactured by MCKESSON TECHNOLOGIES INC.

80010939020013 - McKesson Radiology2018-09-24
80010939020020 - McKesson Radiology2018-09-24
80010939020037 - McKesson Radiology2018-09-24
80010939020044 - McKesson Radiology2018-09-24
80010939120010 - Conserus Enterprise Viewer2018-09-24
80010939120027 - Conserus Enterprise Viewer2018-09-24
80010939130019 - Conserus Enterprise Viewer Mobile2018-09-24
80010939040028 - McKesson Cardiology ECG Management2018-07-06

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