FDA UDI In Commercial Distribution 🇺🇸 United States

CardioDay V2.5

DI: 04250903202445 · Model: Global SP04 · getemed Medizin- und Informationstechnik AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CardioDay V2.5
Primary DI
04250903202445
Version / Model
Global SP04
Catalog Number
2092504-254
Company Name
getemed Medizin- und Informationstechnik AG
Labeler DUNS
331682898
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-29
Public Version
1
Public Version Date
2020-10-07
Public Version Status
New
Public Device Record Key
bdd49f5a-7356-4b73-bc22-40f32589ec2e

Device Description

The CardioDay V2.5 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 V2.5 system is intended to be used by trained operators under the direct supervision of a licensed healthcare practitioner in a hospital or clinic environment.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQK Computer, Diagnostic, Programmable

GMDN Terms

Code Name
35162 Electrocardiographic ambulatory recorder

Identifiers

Type ID
Primary 04250903202445

Premarket Submissions

Submission Number Supplement Number
K162023 000