eudamed_udi Primary ID: G520MD16400

Lucas Curette 4mm (UDI G520MD16400)

Manufactured by Medspo

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lucas Curette 4mm (Model/Catalog Number: MD1640) is a medical device manufactured by Medspo. This product is indexed under FDA Product Code / Category Classification L159001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD1640
Product Code / EMDN: L159001
Device Name: Lucas Curette 4mm
Database Sync Date: 2026-08-09 16:59:33

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 Lucas Curette 4mm?

The registered manufacturer of record for Lucas Curette 4mm is Medspo.

What is the Primary UDI-DI identifier for Lucas Curette 4mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G520MD16400.

What classification code is assigned to this device?

This device is registered under product classification code L159001.

Similar Classification Devices (L159001)

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