eudamed_udi
Primary ID: 08056732651500
Unspecified Brand (UDI 08056732651500)
Manufactured by CARDIOLINE SpA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08056732651500
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: KTCH3000N-E) is a medical device manufactured by CARDIOLINE SpA. This product is indexed under FDA Product Code / Category Classification Z12050302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KTCH3000N-E
- Product Code / EMDN
- Z12050302
- Device Name
- touchECG System config. Windows HD+12 Reusable
- Database Sync Date
- 2026-08-10 05:06:30
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is CARDIOLINE SpA.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056732651500.
What classification code is assigned to this device?
This device is registered under product classification code Z12050302.
Similar Classification Devices (Z12050302)
Other Devices by CARDIOLINE SpA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint