gudid Primary ID: X-9-28-T10-MC

Nexus (UDI X-9-28-T10-MC)

Manufactured by Micro Therapeutics, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Nexus (Model/Catalog Number: X-9-28-T10-MC) is a medical device manufactured by Micro Therapeutics, Inc.. This product is indexed under FDA Product Code / Category Classification HCG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: X-9-28-T10-MC
Product Code / EMDN: HCG
Device Name: Detachable Coil
Database Sync Date: 2026-08-09 09:33:17

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 Nexus?

The registered manufacturer of record for Nexus is Micro Therapeutics, Inc..

What is the Primary UDI-DI identifier for Nexus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is X-9-28-T10-MC.

What classification code is assigned to this device?

This device is registered under product classification code HCG.

Similar Classification Devices (HCG)

Other Devices by Micro Therapeutics, Inc.

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