FDA UDI In Commercial Distribution 🇺🇸 United States

Midmark

DI: 08056732652491 · Model: Midmark Digital ECG · CARDIOLINE SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Midmark
Primary DI
08056732652491
Version / Model
Midmark Digital ECG
Catalog Number
1-100-1550
Company Name
CARDIOLINE SPA
Labeler DUNS
339465174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-05
Public Version
1
Public Version Date
2023-12-13
Public Version Status
New
Public Device Record Key
e9a0d3e3-9eaa-406f-b4ea-4951f35d3db3

Device Description

ECG acquisition capabilities to resting ECG and stress test systems. (Wireless acquisition module)

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

GMDN Terms

Code Name
16231 Electrocardiograph, professional, multichannel

Identifiers

Type ID
Primary 08056732652491