gudid
Primary ID: Midmark Digital ECG
Midmark (UDI Midmark Digital ECG)
Manufactured by CARDIOLINE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Midmark - Primary ID Midmark Digital ECG
Device Regulatory Overview
The Midmark (Model/Catalog Number: Midmark Digital ECG) is a medical device manufactured by CARDIOLINE SPA. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Midmark Digital ECG
- Product Code / EMDN
- DRG
- Device Name
- ECG acquisition capabilities to resting ECG and stress test systems.(Wireless acquisition module)
- Database Sync Date
- 2026-08-09 09:04:28
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Midmark?
The registered manufacturer of record for Midmark is CARDIOLINE SPA.
What is the Primary UDI-DI identifier for Midmark?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Midmark Digital ECG.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
Other Devices by CARDIOLINE SPA
Programmatic Export
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