gudid Primary ID: X-9-18-T10-MC

Nexus (UDI X-9-18-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-9-18-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-9-18-T10-MC
Product Code / EMDN: HCG
Device Name: Detachable Coil
Database Sync Date: 2026-08-09 09:33:17

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 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-9-18-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.

Programmatic Export

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

JSON API Endpoint