gudid Primary ID: 23-174 V1.0 IEC

Unimed (UDI 23-174 V1.0 IEC)

Manufactured by Unimed Medical Supplies, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unimed (Model/Catalog Number: 23-174 V1.0 IEC) is a medical device manufactured by Unimed Medical Supplies, Inc.. This product is indexed under FDA Product Code / Category Classification DSA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 23-174 V1.0 IEC
Product Code / EMDN: DSA
Device Name: One-piece ECG Monitor Cable PARSYS
Database Sync Date: 2026-08-09 09:04:58

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 Unimed?

The registered manufacturer of record for Unimed is Unimed Medical Supplies, Inc..

What is the Primary UDI-DI identifier for Unimed?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 23-174 V1.0 IEC.

What classification code is assigned to this device?

This device is registered under product classification code DSA.

Similar Classification Devices (DSA)

Other Devices by Unimed Medical Supplies, Inc.

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