GUDIDData
gudid Primary ID: 122000500

SC3123 (UDI 122000500)

Manufactured by Esaote Europe B.V.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SC3123 - Primary ID 122000500

Device Regulatory Overview

The SC3123 (Model/Catalog Number: 122000500) is a medical device manufactured by Esaote Europe B.V.. This product is indexed under FDA Product Code / Category Classification ITX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
122000500
Product Code / EMDN
ITX
Device Name
Database Sync Date
2026-08-09 09:04:29

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 SC3123?

The registered manufacturer of record for SC3123 is Esaote Europe B.V..

What is the Primary UDI-DI identifier for SC3123?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 122000500.

What classification code is assigned to this device?

This device is registered under product classification code ITX.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint