eudamed_udi Primary ID: 44560141949377

Unspecified Brand (UDI 44560141949377)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 670 8549) is a medical device manufactured by Konica Minolta, Inc.. This product is indexed under FDA Product Code / Category Classification Z130101 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: 670 8549
Product Code / EMDN: Z130101
Device Name: SD-E
Database Sync Date: 2026-08-09 16:30:30

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 44560141949377.

What classification code is assigned to this device?

This device is registered under product classification code Z130101.

Similar Classification Devices (Z130101)

Other Devices by Konica Minolta, Inc.

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