Lode B.V. (UDI 938902)

Manufactured by Lode B.V.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lode B.V. (Model/Catalog Number: 938902) is a medical device manufactured by Lode B.V.. This product is indexed under FDA Product Code / Category Classification IOL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 938902
Product Code / EMDN: IOL
Device Name: 938902 Valiant 2 sport
Database Sync Date: 2026-08-09 09:26:51

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 Lode B.V.?

The registered manufacturer of record for Lode B.V. is Lode B.V..

What is the Primary UDI-DI identifier for Lode B.V.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 938902.

What classification code is assigned to this device?

This device is registered under product classification code IOL.

Similar Classification Devices (IOL)

Other Devices by Lode B.V.

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