GUDIDData
eudamed_udi Primary ID: 07350135630010

Zenicor View (UDI 07350135630010)

Manufactured by Zenicor Medical Systems AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zenicor View - Primary ID 07350135630010

Device Regulatory Overview

The Zenicor View (Model/Catalog Number: N/A) is a medical device manufactured by Zenicor Medical Systems AB. This product is indexed under FDA Product Code / Category Classification Z12050392 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
N/A
Product Code / EMDN
Z12050392
Device Name
Zenicor-EKG Back-end system
Database Sync Date
2026-08-09 17:06:32

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Zenicor View?

The registered manufacturer of record for Zenicor View is Zenicor Medical Systems AB.

What is the Primary UDI-DI identifier for Zenicor View?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350135630010.

What classification code is assigned to this device?

This device is registered under product classification code Z12050392.

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