eudamed_udi Primary ID: 04560141933200

Unspecified Brand (UDI 04560141933200)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: RC-300 14×17: A3P1) is a medical device manufactured by Konica Minolta, Inc.. This product is indexed under FDA Product Code / Category Classification Z11060280 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2769-2017 View Full Alert →

Diagnostics Ultrasound System Ultrasounds System Sonimage HS1...

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Technical Specifications

Model Number: RC-300 14×17: A3P1
Product Code / EMDN: Z11060280
Device Name: RC-300
Database Sync Date: 2026-08-09 17:43:38

Full Regulatory Attributes

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{
    "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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Konica Minolta, Inc..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04560141933200.

What classification code is assigned to this device?

This device is registered under product classification code Z11060280.

Similar Classification Devices (Z11060280)

Other Devices by Konica Minolta, Inc.

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