CardioDay 2092504-270

GUDID 04250903202520

The CardioDay Holter Analysis Software is designed for the acquisition, analysis, edit, review, report, and storage of ambulatory and multi-parameter ECG data. Results of the automated analysis are intended to assist the physician in the interpretation of the recorded data. This information is not intended to serve as a substitute for the physician overread of the recorded ECG data. The CardioDay system is intended to be used by trained operators under the direct supervision of a licensed healthcare practitioner in a hospital or clinic environment.

getemed Medizin- und Informationstechnik AG

Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder
Primary Device ID04250903202520
NIH Device Record Keye418026f-49ba-4b7b-a09d-1935a8a8e1b6
Commercial Distribution StatusIn Commercial Distribution
Brand NameCardioDay
Version Model Numberv2.7 Global
Catalog Number2092504-270
Company DUNS331682898
Company Namegetemed Medizin- und Informationstechnik AG
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 Datetrue
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
GS104250903202520 [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 Date2023-07-31
Device Publish Date2023-07-21

On-Brand Devices [CardioDay ]

04250903202469The CardioDay Holter Analysis Software is designed for the acquisition, analysis, edit, review,
04250903202520The CardioDay Holter Analysis Software is designed for the acquisition, analysis, edit, review,

Trademark Results [CardioDay]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CARDIODAY
CARDIODAY
79215365 5526814 Live/Registered
getemed Medizin- und Informationstechnik AG
2017-06-14
CARDIODAY
CARDIODAY
79018792 3199080 Live/Registered
getemed Medizin- und Informationstechnik AG
2005-08-04

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