eudamed_udi Primary ID: G520MD45040

Ligature Director Hollow (UDI G520MD45040)

Manufactured by Medspo

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ligature Director Hollow (Model/Catalog Number: MD4504) is a medical device manufactured by Medspo. This product is indexed under FDA Product Code / Category Classification L150701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD4504
Product Code / EMDN: L150701
Device Name: Ligature Director Hollow
Database Sync Date: 2026-08-09 16:46:09

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 Ligature Director Hollow?

The registered manufacturer of record for Ligature Director Hollow is Medspo.

What is the Primary UDI-DI identifier for Ligature Director Hollow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G520MD45040.

What classification code is assigned to this device?

This device is registered under product classification code L150701.

Similar Classification Devices (L150701)

Other Devices by Medspo

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