Change Healthcare Cardiology Hemo

GUDID 17540262100129

Change Healthcare Canada Company

Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer Cardiac catheterization laboratory computer
Primary Device ID17540262100129
NIH Device Record Key10a79fa3-2204-4280-8550-bab2f84392da
Commercial Distribution StatusIn Commercial Distribution
Brand NameChange Healthcare Cardiology Hemo
Version Model Number15.1
Company DUNS246576391
Company NameChange Healthcare Canada Company
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS117540262100129 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQKComputer, Diagnostic, Programmable

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-02-16
Device Publish Date2024-02-08

On-Brand Devices [Change Healthcare Cardiology Hemo]

1754026210004414.3
1754026210005114.3.2
1754026210009915.0
1754026210010515.0.1
1754026210003714.2
1754026210012915.1

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.